Mendel,MD
Toggle navigation
Upload
Dashboard
1-Click
Tools
Filter Analysis
Family Analysis
Comparison
Browser
Data Query
Docs
Forum
Sign in
+ Filter Options
Main
Variants
Databases
SELECT VARIANTS FROM
EXCLUDE VARIANTS FROM
INDIVIDUALS:
sample 1000
na12878 recessive
exome_4_els var annotated
exome_3_eds var annotated
4501349 filtered
stv2_auto_user_qd5-282-stv2_20170530_435_variantreport
a7kcg_miseq3_nih-1_s1
hc082_s4_l001_r_raw
pid616-variant_table
kuhno_1-10 ip_264_1.variant2
kuhno_1-10 ip_264_2.variant3
kuhno_1-10 none.variant
kuhno_1-10 up_218_1.variant
kuhno_1-10 up_218_2.variant
kuhno_1-10 up_218_3.variant
kuhno_1-10 up_218_4.variant
kuhno_1-10 up_218_5.variant
kuhno_1-10 up_218_6.variant
kuhno_1-10 up_218_8_variants_none.variant
nordenskjold_uwcmg_ah_1 hf final 171270
proie_c_prob_raw_snps_indels_hapcall_genotype_filtered_phased g Pesci_M_mother
nordenskjold_uwcmg_ah_1 hf final 171272
nordenskjold_uwcmg_ah_1 hf final 171796
3029
3030
proie_c_prob_raw_snps_indels_hapcall_genotype_filtered_phased g Proie_C_prob
proie_c_prob_raw_snps_indels_hapcall_genotype_filtered_phased g Proie_L_father
5pct_s1-lof
5pct_s1-unified-snp-indle
dnl46897_jcv imported
1313946
tsvc_variants_ionxpress_001
tsvc_variants_ionxpress_002
we_ex1704620
exome_4_els var annotated
genome_ann_shippy_full_20150426064857
73411510240357_annotated
7341maas0357_annotated
genome_mike_maas_v4_full_20170611220637-output
genomapp23a_completereport_20170505
snpsforvep
genome_me_full_20160129125336
paciente_3751_26_mayo_17_26may2017_15_09_01_836
de2670_08232016_bwamem filtered haplotype snpindel
dnn62 snp
dxc01 snp
lfl38 snp
msp09 snp
sp16_multisample SP16_819
sp16_multisample SP16_820
sp16_multisample SP16_961
sp16_819
sp16_961
sp16_820
ba exome
sample_cs2-dmso_recalibrated_variants_snps_only_hard_filtered_snps_only
sample_cs2-enzar_recalibrated_variants_snps_only_hard_filtered_snps_only
trf_44289
8754_onol_s2_vs_onol_n_ucla TUMOR
8754_onol_s2_vs_onol_n_ucla NORMAL
1-p159 final
gird-c1a filtered variants
na12878 dominant
goku_snps_indels
concordancevcf_d5_20161214 GATK-HC_D5
concordancevcf_d5_20161214 Mpileup_D5
concordancevcf_d5_20161214 Pindel_D5
concordancevcf_d5_20161214 FreeBayes_D5
concordancevcf_d5_20161214 VarScan_D5
nk_full_variant_table
kk_full_variant_table
ek_full_variant_table
ldp546
sample 1000
valid-000001933_mtdepth-216 smcounter cut
lb9428 final
vcfbeta-gs000035329-asm
0010dbs 0_bwamem sort rmdup readfiltered realn recal 0_gatk_hc
10 1016j ogc 2015 10
muestra3_s1
muestra2_s1
muestra1_s1
carsonmiller_e4113_h150317_7_mutation_report1-ngs408 10
filter output step4
ngs049p_s3
panvjj_normal_tumor strelka indels gatk annotated NORMAL
panvjj_normal_tumor strelka indels gatk annotated TUMOR
exome_all
54144-mm-ensemble
17nr2143
i26272829p2 hg19_multiannofinal-pacientes-f8765-1-e-f9759-1
manuela_niro
galaxy208-vcfcombine__on_data_201_data_200_and_data_199-1 14cc247
galaxy208-vcfcombine__on_data_201_data_200_and_data_199-1 14cc246
galaxy208-vcfcombine__on_data_201_data_200_and_data_199-1 14cc248
genome_patricia_tachinardi_andrade_silva_v4_full_20170430162109
oje115-001 vqsr all
genome_simone_niciura_v4_full_20170629062030
dipg0076_interval TUMOR
dipg0076_interval NORMAL
gg_mutation_report
ee
grc14378020_exome
grc14378018_exome
grc14378021_exome
grc14378019_exome
grc14378022_exome
family15 variants v3
i29p2-c-18094-iii
h1esc_mtesr1 samtools indel
test
v2649_v1_non-filtered_2017-07-24_10_39_21
v2649_v1_non-filtered_2017-07-24_10_39_21
62393865_s40 mvar 62393865_S40.FREEBAYES
62393865_s40 mvar 62393865_S40.GATK
62393865_s40 mvar 62393865_S40.SAMTOOLS
cmi
ppox
ppox
nextera4_03 03 2017_brca_13_s13_v5
hg001_grch37_giab_highconf_cg-illfb-illgatkhc-ion-10x-solid_chrom1-x_v 3 3 2_highconf_pgandrtgphasetransfer
tsc_27 01 2017_8_s8_v7
tsc_27 01 2017_8_s8_v7
cmt4
larissa_s11
myexome-1
c002_attactcg-tatagcct srt mkdups flt
c003_attactcg-atagaggc srt mkdups flt
c005_attactcg-cctatcct srt mkdups flt
final-ma145
mpe115_v1112
pep_0060
gordonsepilepsy filtered 2076
gordonsepilepsy filtered 2077
gordonsepilepsy filtered 2484
gordonsepilepsy filtered 2486
gordonsepilepsy filtered 2487_pool
gordonsepilepsy normalized 2076
gordonsepilepsy normalized 2077
gordonsepilepsy normalized 2484
gordonsepilepsy normalized 2486
gordonsepilepsy normalized 2487_pool
outputvcforig-sve05k
12ac02301-1_s1 genome
13ac00301-2_s1 genome
15ac02301_s1 genome
15ac02302_s1 genome
15ac02302_s1 genome
15ac02303_s1 genome
2-ac-cap17_s1 genome
15ac02301_s1 genome
15ac02303_s1 genome
15ac02303_s1 genome
16hpc01701_s1 genome
16hpc01702_s1 genome
16hpc01703_s1 genome
15a02301_s1 genome
09pla02101_s1 genome
zehra_acar_variant_analysis_report-2
genome_adam_cuomo_v4_full_20170809151438
sl85 samtools snp
gpp10314_20120828021333_nucseek
gpp10315_20120828021333_nucseek
genome_none_none_v4_full_20170814115900 Aug
genome_none_none_v4_full_20170814115900 14
genome_none_none_v4_full_20170814115900 11:59:00
genome_none_none_v4_full_20170814115900 2017
variant_list
l-322-filtered-snps-indels
16on271_ionxpress_012
eb408_unique
eb409_unique
myexome-1 annotated mendelmd
myexome-1 annotated mendelmd
idash_ishimaki
idp34_annotado
combined sample_100.variant
combined sample_38.variant2
combined sample_39.variant3
combined sample_40.variant4
combined sample_41.variant5
combined sample_42.variant6
combined sample_43.variant7
combined sample_44.variant8
combined sample_45.variant9
combined sample_46.variant10
combined sample_47.variant11
combined sample_48.variant12
combined sample_49.variant13
combined sample_50.variant14
combined sample_51.variant15
combined sample_53.variant16
combined sample_54.variant17
combined sample_55.variant18
combined sample_56.variant19
combined sample_57.variant20
combined sample_59.variant21
combined sample_60.variant22
combined sample_61.variant23
combined sample_62.variant24
combined sample_63.variant25
combined sample_64.variant26
combined sample_66.variant27
combined sample_67.variant28
combined sample_68.variant29
combined sample_69.variant30
combined sample_70.variant31
combined sample_71.variant32
combined sample_72.variant33
combined sample_73.variant34
combined sample_74.variant35
combined sample_91.variant36
combined sample_92.variant37
combined sample_93.variant38
combined sample_94.variant39
combined sample_95.variant40
combined sample_96.variant41
combined sample_97.variant42
combined sample_98.variant43
combined sample_99.variant44
mt2379_s1
fyc5
dna-data-2017-08-27
isabela
g104-1_bowtie2_dupremoved_realigned_v0 1 19mpileup_dummy
anemia
a_kheyri final
pytbv dbsnpa
1445140
46651510241455_annotated
mm170802ap
an035_hg19
allfamilies AWI
allfamilies AWJ
allfamilies AWK
allfamilies AWL
allfamilies AWM
allfamilies BIR
allfamilies BQ0
allfamilies BIP
allfamilies BIQ
fam3 AWI
fam3 AWJ
fam3 AWK
n498_snp_indel_anno
sample13_s1_s1_001_filtered_dp10_splitted
sample14_s2_s2_001_filtered_dp10_splitted
sample15_s3_s3_001_filtered_dp10_splitted
p0085_filtered
variants
refseq_hg38_cds merged symbol igv-capture hist coverage
chu17257-cha-zoe_s2
full_genome
15071143293692125889425
1507114365681-1642853908
genome_tim_dotson_v5_full_20171008065907
genesmarker
mitovcf_file
snps raw-snps 17_0233
snps raw-snps 17_0234
snps raw-snps 17_0235
62408779_s7 mvar 62408779_S7.FREEBAYES
62408779_s7 mvar
62408779_s7 mvar 62408779_S7.GATK
62408779_s7 mvar 62408779_S7.SAMTOOLS
genome_christian_muller_v3_full_20161102032233
genome_christian_muller_v3_full_20161102032233
genome_christian_muller_v3_full_20171011070154 Oct
genome_christian_muller_v3_full_20171011070154 11
genome_christian_muller_v3_full_20171011070154 07:01:54
genome_christian_muller_v3_full_20171011070154 2017
ashksample HG002
ashksample HG003
ashksample HG004
mpileup-final_calls_32716
ioncode_0105_fn25 bam-25 IonCode_0105_FN25.bam
ioncode_0105_fn25 bam-25 [25]
ioncode_0105_fn25 bam-25 (single)
ioncode_0105_fn25 bam-25 (Reads,
ioncode_0105_fn25 bam-25 Locally
ioncode_0105_fn25 bam-25 Realigned,
ioncode_0105_fn25 bam-25 Variants,
ioncode_0105_fn25 bam-25 EXON,
ioncode_0105_fn25 bam-25 AAC,
ioncode_0105_fn25 bam-25 AIFOG)
17-11096s1 germline-multisample gatk annotated 17-11096s1
17-11096s1 germline-multisample gatk annotated 17-11097s2
17-11096s1 germline-multisample gatk annotated 17-11098s1
17-11096s1 germline-multisample gatk annotated 17-11099s1
dossier4-di450-2-b00h4r3_hg19_snp annot
r_2016_06_15_14_03_10_user_mx-267-exomess_pool37_5b552 570 872
5500xl_23312002_2013_06_25_exomas16_2h495 processed recal
5500xl_23312002_2013_06_25_exomas16_2h496 processed recal
ca
snps raw-variants selected
snps raw
71161510240931_annotated-4
fakhrieh_salemi gatk snp
fakhrieh_salemi gatk snp
index31
fakhrieh_salemi gatk indel
filter output step3
chh6738_annovar
82937_v1
5840_s17
5516_s23
75_filt_10x
15001702300578a snp-1
qw2315_combined_r1 fastq raw
62388010_s7 mvar 62388010_S7.FREEBAYES
62388010_s7 mvar 62388010_S7.GATK
62388010_s7 mvar 62388010_S7.SAMTOOLS
eb1954_unique
f1 H02H9ALXX_1_F01_K0512P_Human_NoIndex_2-25348_Spuler_Lab_R1
f1 (paired)
f1 trimmed
f1 (paired)
f1 (Reads)
f1 -
f1 locally
f1 realigned
f1 (Variants,
f1 AAC)
allllllllllllyblswd
pdb336 vep
pdb346 vep
327_c879tanxx_gatagaca_l005 bam filtered vep Protein_position
327_c879tanxx_gatagaca_l005 bam filtered vep Amino_acids
327_c879tanxx_gatagaca_l005 bam filtered vep Codons
327_c879tanxx_gatagaca_l005 bam filtered vep Existing_variation
327_c879tanxx_gatagaca_l005 bam filtered vep Extra
339_c879tanxx_aaggacac_l005 bam filtered vep Protein_position
327_c879tanxx_gatagaca_l005 bam filtered vep Protein_position
pg_merged_chr19 recode PG1
339_c879tanxx_aaggacac_l005 bam filtered vep Amino_acids
327_c879tanxx_gatagaca_l005 bam filtered vep Amino_acids
327_c879tanxx_gatagaca_l005 bam filtered vep Codons
339_c879tanxx_aaggacac_l005 bam filtered vep Codons
339_c879tanxx_aaggacac_l005 bam filtered vep Existing_variation
327_c879tanxx_gatagaca_l005 bam filtered vep Existing_variation
327_c879tanxx_gatagaca_l005 bam filtered vep Extra
339_c879tanxx_aaggacac_l005 bam filtered vep Extra
pg_merged_chr19 recode PG2
pg_merged_chr19 recode PG3
pg_merged_chr19 recode PG4
tz1
tz1
wes_0001 hg19 bwa gatk freebayes combined
fam5 cleaned 3403_16
fam5 cleaned 3404_16
fam5 cleaned 3405_16
fam5 cleaned 3422_16
variants default
variants default
variants default
variants default
cds 3403_16
cds 3404_16
cds 3405_16
cds 3422_16
snps raw-variants selected 3403_16
snps raw-variants selected 3404_16
snps raw-variants selected 3405_16
snps raw-variants selected 3422_16
tsvc_variants_ionxpress_032
24_genetics_snv_99 8 slt
b12
1528098
damold_variant
damold_variant
tumor_sample brca
t30541_annotated_calls
t30541_annotated_calls
tumor_sample brca
nipe_alignment snps
halo_cad_march_17
halo_cad_march_17
mm170835gc
mm171122md
261_emreatak_v1_non-filtered_2016-09-01_06_25_23
upload2ensembl
snps raw MG15-000
snps raw MG15-001
snps raw MG15-002
snps raw SHA-06-33146
watson
sg5_onco_2_s2_v13
rawdata23andme
fam001 NG171210431
fam001 NG171210432
fam001 NG171210433
tsc_7_5_s5_v13
5_s5
5_s5 genome
trio_parsed_vcf15_03359procol_vcf_report overall_15_03359procol_R1_converted_Unique_Output.pjt
trio_parsed_vcf15_03359procol_vcf_report 15_06810matcol
trio_parsed_vcf15_03359procol_vcf_report 15_06811patcol
na12878 recessive
ex-15004
fpd-aix-mes-312-12
fpd-alg-mad-1230-3
jg31048rm_filtered-jrmeena-copy 117543
5517_sorted_hg19
example_snp
er-447_an6 ann hg38_multianno_umd
na12878 compound_heterozygous
552117_ngs_ex
552017_ngs_ex
552217_ngs_ex
annotation final
552217_ngs_ex annotated mendelmd
miller
abdullah_h_mahmood_ngs_032_17 ionxpress_011 r_2017_11_03_08_01_58_user_s5-0138-35-copy_of_ngs_032_17_aip_48_ornek_2
mm180101la
mm180104ea
mm180106mm
mm180110lp
mm180111m
mm180112f
1_s1 genome
1_s1
1_s1
2_s2
3_s3
4_s4
hboc12
10049_haplotypecaller_target
hgcat_input_example-3
child2_indexed
ptc-wgs combined vep gnomad
dels
d233
cpt10
33011510240923_annotated
amal-report-2
073_tsvc_variants
046_tsvc_variants
045_tsvc_variants
044_tsvc_variants
043_tsvc_variants
042_tsvc_variants
033_tsvc_variants
031_tsvc_variants
030_tsvc_variants
sm006-1 both
sm007-1 both
sm008-1 both
55001703319634a raw
01pjhc5_s1_l001_r0trimunpaired_cut_fastqc
01pex6c4_s1_indel_filter_end
mm180211ms
aml-1726_v1_non-filtered_2017-02-26_03_51_07
gt_so_4086_igt_1r
index13_otb1697_gerard goyette_500-049a_human_hex_av5-utr_50x_03232016 deduplicated realigned recalibrated snpeff snpsift
index9_otb1693_gerard goyette_500-049a_human_hex_av5-utr_50x_03232016 deduplicated realigned recalibrated snpeff snpsift
index34_otb3338_gerard goyette_500-049a-2_human_hex_av5-utr_50x_06112016 deduplicated realigned recalibrated snpeff snpsift
18063
21_s21
nist_integratedcalls_12datasets_130517_hethomvarpass_vqsrv2 15
21_s21 genome
gfg_filtered_unphased_genotypes_vcf
schinzel_giedion
432 varscan snp snpann
mng17-30918-p-lin003-patient-0001-e9504_mutation_report1
n2_s17
tsvc_variants_ionxpress_001
tsvc_variants_ionxpress_004
lanjinglingc2017103103501 mkdup sorted genotypegvcf
mmg003343
hodakb10_snp_indel_anno
hodakb12_snp_indel_anno
hodakt10_snp_indel_anno
hodakt12_snp_indel_anno
patient ann filtered
62334902_s25-161111_k00359_0038_bhg532bbxx-normal-illuwes-4f0ca40f-mvar
62334902_s25-161111_k00359_0038_bhg532bbxx-normal-illuwes-4f0ca40f-mvar
mp91583 both
ancestrydna
el-exome_s1
tsvc_variants_ionxpress_001-5225
9040 snpeff high
9040 cleaned_snpindel
9040 snpeff moderate
ex_013_mod
94533-0209701724_ms_onbait
promethease-1
71161510240931_annotated-4
hsp116-ii-1-filtered_variants
annovar hg19_multianno_pass
miller snpeff
s308
s315_9
248419675_annotated
test
variants
tsvc_variants_ionxpress_002-4
tsvc_variants_ionxpress_002-4
annotation final
ex
ex-sf
tsvc_variants_ionxpress_040
ap253-3 final
aaa
acacia
filtered
scz009_trimmed samtools
dnl109758_dez imputed
output 09_chr1 fa filtered3
45655-cr-ensemble
galaxy103-varscan_on_data_102
test
m1_rms1_10
m1_rms1_1
m1_rms1_11
m1_rms1_12
m1_rms1_14
m1_rms1_15
m1_rms1_13
m1_rms1_16
m1_rms1_17
m1_rms1_18
m1_rms1_19
m1_rms1_3
m1_rms1_2
m1_rms1_5
m1_rms1_4
m1_rms1_6
m1_rms1_7
m1_rms1_8
m1_rms1_9
mm180725at
mm180706dm
img-20181008-wa0006
tcga-bf-a1pu-01a-11d-a19a-08
pbrpl18h2_-_sravanthi_filtered_2018-09-27_04_08_32
breast1 1
sample1
mo-mi-abdi1130 final
u697_bwa_picard
164649418_s1 ann select dbsnp
na12877-rep1_s1
na12877-rep1_s1
f txt
f
2-fl-ha_482-01
miller
ctr0100487_mex076_alain_mancinas_201814015100_pass
bra19324freebayes
traning-sample-vcf-file
lapatrada pol indel
22603_s43
22603_s55
ns1-6
ns1-5 final
ns2-5 filtered variants
ns2-10 final
ns4-4
ns4-5
ns4-6
sama-karam_s1
copy-of-pof-ii-1-filtered-snps-indels-query output genome_summary
hsp108-ii-1-filtered_variants
2636_s28
2761_s29
4450_s11
6306_s1
6343_s27
6422_s23
6424_s25
6426_s21
12016_s26
12030_s5
12061_s9
12066_s20
12067_s13
12068_s19
12078_s17
12083_s14
12086_s22
12092_s33
12107_s6
16420_s8
16431_s7
16441_s18
17503_s31
17507_s32
2632_s12
sy-51_s2
sy-52_s3
2632_s12
2632_s12
jp5186_chip
32
na12878 dominant
miller
filtered_merged_a00k
rm-274 final
pm-286 final
diu946-001_results_diu946-001 final
shr
genome_jeffrey_bloom_v5_full_20190110052330
genome_jeffrey_bloom_v5_full_20190110052330
ht12d final
gatk f008 reheader
father
sec-2-18-7_filtered
sample_file
wanguard_s1
cdh6-52
full_combined_excel
miller
my var-final
62455815_s29 mvar
tsvc_variants_ionxpress_002
59876-as-ensemble
59876-as-ensemble
rf3717
56001801068581a snp
56001801066395a snp
56001801066395a indel
fmsd_filtered_snp_indel
180919fr-013-1
tsvc_variants_ioncode_0249
37-g0191 raw_variants
mr
mr
wes 6160 filtered recode
1886106_bak chr20
genome_susan_abernathy_v4_full_20190218171918
drift-nimh_freeze2_brmenn
9etks0122_annotation
17on508_ioncode_0113
a-full_variant_table
gm12878
hd829_190221_nb551050_0207_ahvwygbgx9 germline
solo_-a-star-wars-story-trailer
ctr0100514_mex083_jonathan_resendiz_20190502090400_pass
ctr0100502_mex079_amisaday_mora_20190330015800
200567_mutation_report1_filtered
qmul_trio_lof_assignment_2019
sample_hardfiltered
trio2 snpeff canon annotated exons dhg21091-v
trio2 snpeff canon annotated exons dhg21610-v
trio2 snpeff canon annotated exons dhg21611-v
8wkyncwo
8wkyncwo
mm160117hb v200
skaz004 gatk snp
porto_final_annot intervar_annovar
53586-full_variant_table
53586-full_variant_table
dna-data-2019-03-03
60820188484921_wgz snp-4
gi-variants-passed-homoz
wes_0012 hg38
rcl1126
wt108005 snp
wt108005fu0 snp
wt108005mu0 snp
mm190528hvp
mm190623opd
myexome
54871510242650_annotated-2
aghdas_dehghani qualified
plink
filtered4
filtered2
filtered5
filtered6
mpileup-final_calls_arg_046
111
p001_fim
xah
2_s2
kemikp79
h8m mutect2
001 final
60820188472738 snp
allsamples as snp_indel_pass_annotated
h7 indel_final
h11 snp_final
ashwath_ramji_slb567__wes_annotated_vcf
60820188484090 snp
56001808052608_wgz sv
f70
mr50 2
60820188481224 snp
60820188481224 indel1
yushu_s1 hg19_multianno
lh-2005601_umi hg19_multianno
pcg-f60 allchr snpeff p sal sal10_1 clinvar candidate_genes_tagged
genom_v5_full_20190304173844
144336383-full
144336383-full
moss final
62421900_s18-180124_k00541_0065_bhnjl7bbxx-normal-illuwesagi-76f236ce-freb filt pass
mmcs-209a
trio 2010_06 ychr sites-v2
trio 2010_06 ychr sites-v2
trio 2010_06 ychr sites-v2
file
tsvc_variants_ionxpress_006
f204-1528-proband
f204-1533-proband2
f204-1533-proband2
f204-1533-proband2
cp00040635 filtered indel
cp00040635 filtered snp
s216 g
6-na1287 both
00126 vep
demo1
60820188477917 filtered snp
f000043987_dp5_tag
2019_09_14t01_36_55z_suma_ionxpress_003
azm002
19508-01-01_s2
mm005
bm011
193810-bpl33-fg3374-sal-pi-19-16-4228-rhamppcr2_s123_l001_q20l30_sorted_primtv_snps
dg001 final
83356 33710_s2 smcounter anno
07-ms_s7 filtered vt snps indels annotated hg19_multianno
08-dh_s8 filtered vt snps indels annotated hg19_multianno
09-gf_s9 filtered vt snps indels annotated hg19_multianno
06t10508_snvintersect
95t14234_snvintersect
hht25
60820188482844 cnv
galaxy4-vcfselectsamples__on_data_1
62644690_s62 hpcl fboth pass
62644690_s62 bcfc filt pass
drift-nimh snps indels vqsr qced
62644690_s62 hpcl fboth pass
62644690_s62 bcfc filt pass
chan_pitt final
leila somatic
43_s43
44_s44
30_s30
nunez_a-2
variants selected
variants selected
liw
liw
nba852-001 variants
selected variants chr6
selected variants chr6
1351s
1352s
1353s
genome_aaron_hill_v3_full_20191101162607
skeletal
vqsr_snp_indel hc recaled
out
fomiga
94310feb
94410feb
718
chnaka
udp2568_axeq_1_hs37d5_remdup-uniqmap
udp5436_axeq_1_hs37d5_remdup-uniqmap
udp2569_axeq_1_hs37d5_remdup-uniqmap
udp2570_axeq_1_hs37d5_remdup-uniqmap
udp5435_axeq_1_hs37d5_remdup-uniqmap
udp2568_axeq_1_hs37d5_remdup-uniqmap
udp5436_axeq_1_hs37d5_remdup-uniqmap
udp2569_axeq_1_hs37d5_remdup-uniqmap
udp2570_axeq_1_hs37d5_remdup-uniqmap
sleepdisorders_saxena_sleep_exome_
funcotator_output
pjgl final
s75952_filtered_snps_and_indels
s75952_filtered_snps_and_indels
gen_coords_2546da25
gen_coords_4297ccf5
gen_coords_e4ad64d7
gen_coords_2546da25
gen_coords_2a24f493
20191018_null_jozsefpocsai_1_vcf
alves-daniel
ibg-2-cgm-0130 final
20041952_fiebersyndrome
axiomgt1 calls
136
914
914
dk31-akp-run025
wes413_annotated hg19_multianno
20159-01-01_s13-kopie
20160-01-01_s14-kopie
20160-02-01_s15-kopie
20161-01-01_s16-kopie
20162-01-01_s17-kopie
20163-01-01_s18-kopie
20165-01-01_s19-kopie
20166-01-01_s20-kopie
20167-01-01_s21-kopie
20168-01-01_s22-kopie
sano-converted-xao3oovlc7fnhcwi
60820188481023_wgz sv
nb26r3b7-vcf
nb26r3b7
nb26r3b7-vcf
ca-full_variant_table
df-full_variant_table
il-full_variant_table
le-full_variant_table
p767-full_variant_table
pa883-full_variant_table
p545-full_variant_table
p38bis-full_variant_table
2-pd
15_s15
17_s17
18_s18
mm200519jpm
mm200520lff
002-64854-300-scex
vep
haplotypecaller normalized sort
60820188477428 filtered snp
metin-yusa-ezelsoy
tsonexp104
na12878 recessive
f06400088-ib-ex-60-1639-mahdi-papolzaee-x_s46 soft_filtered
1jzxjfqlmt6b6sjn
sg8_171109_m03874_0051_000000000-bc4b6_osteo_7_s7_v13
2388
2388_2
mm200704jip pass
mm200801fps
mm200802avc
mm200803lca
pa_1_filt_10x
pa_2_filt_10x
pa_2_filt_10x
pa_3_filt_10x
pa_4_filt_10x
tsvc_variants_ionxpress_032
tsvc_variants_ionxpress_029
tsvc_variants_ionxpress_028
tsvc_variants_ionxpress_027
christinas-dna-raw-data
christinas-dna-raw-data
f06400419-ib-ex-34-1651-narges-nikzad-x-7d5-orion-ilya-1_s17 soft_filtered-1
257_mg_v1
ancestrydna
h06400150-ib-ex-60-1801-aliasghar-faghan-tonaj-x soft_filtered
g06400841-ib-ex-60-1790-lia-amanlo-x_s18 soft_filtered
h06400082-ib-ex-60-1795_s23 soft_filtered
g06400842-ib-ex-60-1791_s19 soft_filtered
h06400150-ib-ex-60-1801-aliasghar-faghan-tonaj-x soft_filtered
rbna2s annoted
mm200818ekc pass
60820188476706_wgz snp
60820188477428 filtered snp
60820188477428 filtered indel
mt9975_s20b_raw_onlyvariants
nb4y474q
chr1_tb
chrx_tb
f06400088-ib-ex-60-1639-mahdi-papolzaee-x_s46 soft_filtered
62716307_s105-200325_a00853_0090_bhnncndmxx-normal-illuwestwist-c50063e5-mvar
56001801068832b_wgz indel
56001801068832b_wgz snp
i06400152-ib-ex-60-1844-ehsan-ilya-biotech-orion-raw-data-9-ilya-biotech-4_s237 soft_filtered
data_trios
child filtered_variants
father filtered_variants
mother filtered_variants
raha-nazari
i06401043-ib-ex-60-1962-parsa-riazi-ilya-biotech-100x-7d5-4_s155 soft_filtered
2039528
cypcyp_20170119
lf7070
4k20002_01 gatk
myheritage_raw_dna_data
inbound8305150685853676453
42171
42440
94231510241520_annotated
lscsousa-37862-convertido
db-142035-19648
62792253_s65 bcfc filt pass
li29247
dnl435773_hfn
mm2
genome_benjamin_beeler_v5_full_20201120080226
genome_benjamin_beeler_v5_full_20201120080226
mn1_1_dkdn200006670-1a_hhwwtdsxy_filt_10x
dnaroberta
vcf2
s2421nr2_snvs
2020-005022-full_variant_table
k06401019-ib-ex-60-2014-fateme-pour-orion-raw-data-ilya-biotech_s3 soft_filtered
1351s
1352s
1353s
1352s
1351s
dnl415328_mwu
premaidha_pandita
8_s8
casescomb_anno_nochr vep
controlcomb_anno_vep
013 final
013 final
a1 mutect somatic snv mm10_multianno
a2 mutect somatic snv mm10_multianno
a3 mutect somatic snv mm10_multianno
a4 mutect somatic snv mm10_multianno
a5 mutect somatic snv mm10_multianno
mm210202rsv
mm210206egs
mm210202rsv
example-4 1-bnd
55101705103716_annotated
15001711234580a snp
merged_pe_ann-1
galaxy43-snpeff_eff__on_data_37
60820188472777 cnv
xyk885-001
galaxy6-vcffilter__3022nr6
galaxy6-vcffilter_3022nr4
galaxy7-vcffilter_3022nr8
galaxy7-vcffilter__3022nr7
galaxy36-vcffilter__3466nr4
galaxy7-vcffilter__3466nr40
a
hocanf12689796 cnvnator filter reheader
schinzel_giedion
galaxy7-vcffilter__3466nr3
galaxy7-vcffilter__3466nr4
galaxy7-vcffilter__3466nr40
galaxy7-vcffilter__3466nr42
dados_brutos_saude
dna
20tes0779_fb
frasc37
15001711232689a snp
04-cn_s4
etb21-ktww
genome
wes08-paw final
10200154963-unkown-ib-ex-60-2156-amirreza-safavi-orion-raw-data-9d375-1_s67 soft_filtered
ng11yhb2uc
104001164731-unkownib-ex-60-2253ariyaeskandari-orion-rawdata-9d5-2_s86 soft_filtered
smallvariants filtered
m21 14_15b68a
file
dados_brutos_saude
galaxy8-vcffilter_3910nr1
c1-bcemep2073 snp indel excludeflt grch38
p1-bcemep2058 snp indel excludeflt grch38
c1-bcemep2073 snp indel excludeflt grch38
p1-bcemep2058 snp indel excludeflt grch38
ngs_variants
sample202111_ merge
fls_f1
fls_f1
abdelali_rgd43_1_s22_qualfilter2
89896
mm210618mmm
mm210618mmm
1_1-200000_1234n
62466786_s45 mvar
62466786_s45 mvar
filter output step1
468f2at-raw_hg19
dados_brutos_saude
snp_m4n4
ztc634-001 cnv grch38
ztc634-001 variants grch38
riya_final_variants
rajesh_father_final_variants
riya_sister_final_variants
sweety_das_mother_final_variants
hervkucsc final_compsc12
hervkucsc final_compsc13
hervkucsc final_compsc15
hervkucsc final_compsc16
hervkucsc final_compsc17
hervkucsc final_compsc18
hervkucsc final_compsc21
hervkucsc final_compsc22
hervkucsc final_compsc23
hervkucsc final_compsc24
hervkucsc final_compsc25
hervkucsc final_compsc26
hervkucsc final_compsc27
hervkucsc final_compsc28
hervkucsc final_compsc29
hervkucsc final_compsc30
hervkucsc final_compsc8
hervkucsc final_compsc10
hervkucsc final_compsc11
hervkucsc final_compsc9
hervkucsc final_compsc7
hervkucsc final_compsc2
hervkucsc final_compsc4
hervkucsc final_comp31
haplotypecaller_300_21
sl476778 qc recode
mm210921mll
vcffilter4321nr2
vcffilter4321nr1
c82258b6-cab8-419f-9847-26d3cb04de6c
gowrish_ghosh_7071491
lmivty4833qdq7qw
mk265 final
mk264 final
mk266 final
mk268 final
mk267 final
mm211102rsf
srr8898194
pai-convertido
genera-pai-dados-brutos
23andme
patient
lofreq1-annotation
meu-dna-convertido-v5
f83-1371_s1
f83-980_s1
f83-981_s1
test
test
15001710502500a snp
15001710502500a indel
tw-001-300447370701 hard-filtered
tw-001-300447370801 hard-filtered
tw-001-300447370901 hard-filtered
tw-001-300447371001 hard-filtered
pfeiffer-singleton
igb85_p_baserecal_precalread_varcall g
garrettgeminiuc-ng1kmmceb1-30x-wgs-sequencing_com-10-12-21 mito
eticket_ven014_12191851_1
wes018-ban final
wild final
15001711234580a snp
galaxy396-snpeff_eff__on_data_20_and_data_390
galaxy413-snpeff_eff__on_data_20_and_data_412
test
vars_mtec_s13
readme
153751
tm-001-300470609201_sample-4 hard-filtered
multisample final
all annotation 21
148225_eymennacar_93_final
sec5
galaxy13-vcffilter__on_data_11
myheritage_raw_dna_data
genome_kristen_hiser_v5_full_202204271056061
1ng1gd5leyg-1
output
output
documento-de-eunice
tm-001-300484487501-r1 hard-filtered
tm-001-300484487601 hard-filtered
ngs-5_s2
tw-001-300447371501 hard-filtered
tw-001-300458116301 hard-filtered-2
tm-001-300484487801 hard-filtered
mn1_1_dkdn200006670-1a_hhwwtdsxy_filt_10x
mn1_1_dkdn200006670-1a_hhwwtdsxy_filt_10x
bac931-001 variants grch38_
my_protein_filter_vep
drr006760 haplotypecaller
s65_cosmic_annovar hg38_multianno hg38_multianno
s96_cosmic_annovar hg38_multianno hg38_multianno
hsm03
paolo_maccallini_snp
paolo_maccallini_indel
tomkooy-ng1k4katmj-30x-wgs-sequencing_com-09-09-22 snp-indel genome
15001710502500a snp
na12878 compound_heterozygous
na12878 compound_heterozygous
na12878 compound_heterozygous
kemik154
2765 filtered indel
2765 filtered snp
rawdataoriginal
upj-1_annotation
gen1
63084816_s277 hpcl fboth pass
dados_brutos_423_saude
dados_brutos-fer_212_saude
liblalt53_variants funcotatedb37
ng1hpy2syw1
s_25_17 haplotypecaller filtered
damb121 variants
galaxy94-snpeff_eff__dt-sc1_filtered___100
test
test
variants_1132761_1003714
exome_tobias_qualls_7875dc_e9i96r
epf23-lugp final
mk266 final
mk265 final
mk264 final
mk268 final
mk267 final
freebayes-on-259-variants
br_2009 hard-filtered
88_1_4113063-4113122_fullgenome
88_1_4113063-4113122_fullgenome
sis-3299335378-52-a3-0222-full_variant_table
1-ng10uyr74p-30x-wgs-sequencing_com-01-16-24 snp-indel genome
leftfiltered
leftfiltered
wd_h final
lis_hg19 filt
62951226_s22 bcfc filt pass
62951226_s22 bcfc filt pass
63239608_s186 hpcl fboth pass_2
anotado
SNP LIST:
GROUPS:
3029
3030
test
LG_GGB_20171101
SAVED GENE LIST:
93 genes
A
A
Ataxia
Atypical Hemolytic-Uremic Syndrome
CGH_AR
Childhood Renal panel
chronic nephrotic
CK
comprehensive kidny
Comprehensive Neuromuscular Disorders Panel
Congenital Disorders of Glycosylation Panel
Deb
DEB.ING
Dermatology Gene Panel
Diabetes
Ehler D
Epidermolysis Bullosa 2
Epidermolysis Bullosa Panel
epilepsy
Facial Dysostosis Panel
fanconi
Genes Got Time
HLA
HUS
Hypokalemia and Related Disorders Panel
Ichthyosis
ichthyosis2
ichthyosis3
immunodeficincy
jr
mayoclinic PN
metabolic
Mody
musclat dystrophy
Nada autosomal ressicev
nephrolithiasis
Nephrotic
Neurofibromatosis
Neuropathies
Neuropathies2
Neuropathies 3
ostiopetrosis
perxosomal
primary immunodef
Retinal Dystrophy
SEMD2
Skin and Connective Tissue Disorders Panel
SMED
Spastic Paraplegia
Spinal Muscular Atrophy
Stickler
thrompocytopenia
Treacher Collins syndrome
Treacher Collins syndrome2
white matter disorder
GENE LIST:
INDIVIDUALS:
sample 1000
na12878 recessive
exome_4_els var annotated
exome_3_eds var annotated
4501349 filtered
stv2_auto_user_qd5-282-stv2_20170530_435_variantreport
a7kcg_miseq3_nih-1_s1
hc082_s4_l001_r_raw
pid616-variant_table
kuhno_1-10 ip_264_1.variant2
kuhno_1-10 ip_264_2.variant3
kuhno_1-10 none.variant
kuhno_1-10 up_218_1.variant
kuhno_1-10 up_218_2.variant
kuhno_1-10 up_218_3.variant
kuhno_1-10 up_218_4.variant
kuhno_1-10 up_218_5.variant
kuhno_1-10 up_218_6.variant
kuhno_1-10 up_218_8_variants_none.variant
nordenskjold_uwcmg_ah_1 hf final 171270
proie_c_prob_raw_snps_indels_hapcall_genotype_filtered_phased g Pesci_M_mother
nordenskjold_uwcmg_ah_1 hf final 171272
nordenskjold_uwcmg_ah_1 hf final 171796
3029
3030
proie_c_prob_raw_snps_indels_hapcall_genotype_filtered_phased g Proie_C_prob
proie_c_prob_raw_snps_indels_hapcall_genotype_filtered_phased g Proie_L_father
5pct_s1-lof
5pct_s1-unified-snp-indle
dnl46897_jcv imported
1313946
tsvc_variants_ionxpress_001
tsvc_variants_ionxpress_002
we_ex1704620
exome_4_els var annotated
genome_ann_shippy_full_20150426064857
73411510240357_annotated
7341maas0357_annotated
genome_mike_maas_v4_full_20170611220637-output
genomapp23a_completereport_20170505
snpsforvep
genome_me_full_20160129125336
paciente_3751_26_mayo_17_26may2017_15_09_01_836
de2670_08232016_bwamem filtered haplotype snpindel
dnn62 snp
dxc01 snp
lfl38 snp
msp09 snp
sp16_multisample SP16_819
sp16_multisample SP16_820
sp16_multisample SP16_961
sp16_819
sp16_961
sp16_820
ba exome
sample_cs2-dmso_recalibrated_variants_snps_only_hard_filtered_snps_only
sample_cs2-enzar_recalibrated_variants_snps_only_hard_filtered_snps_only
trf_44289
8754_onol_s2_vs_onol_n_ucla TUMOR
8754_onol_s2_vs_onol_n_ucla NORMAL
1-p159 final
gird-c1a filtered variants
na12878 dominant
goku_snps_indels
concordancevcf_d5_20161214 GATK-HC_D5
concordancevcf_d5_20161214 Mpileup_D5
concordancevcf_d5_20161214 Pindel_D5
concordancevcf_d5_20161214 FreeBayes_D5
concordancevcf_d5_20161214 VarScan_D5
nk_full_variant_table
kk_full_variant_table
ek_full_variant_table
ldp546
sample 1000
valid-000001933_mtdepth-216 smcounter cut
lb9428 final
vcfbeta-gs000035329-asm
0010dbs 0_bwamem sort rmdup readfiltered realn recal 0_gatk_hc
10 1016j ogc 2015 10
muestra3_s1
muestra2_s1
muestra1_s1
carsonmiller_e4113_h150317_7_mutation_report1-ngs408 10
filter output step4
ngs049p_s3
panvjj_normal_tumor strelka indels gatk annotated NORMAL
panvjj_normal_tumor strelka indels gatk annotated TUMOR
exome_all
54144-mm-ensemble
17nr2143
i26272829p2 hg19_multiannofinal-pacientes-f8765-1-e-f9759-1
manuela_niro
galaxy208-vcfcombine__on_data_201_data_200_and_data_199-1 14cc247
galaxy208-vcfcombine__on_data_201_data_200_and_data_199-1 14cc246
galaxy208-vcfcombine__on_data_201_data_200_and_data_199-1 14cc248
genome_patricia_tachinardi_andrade_silva_v4_full_20170430162109
oje115-001 vqsr all
genome_simone_niciura_v4_full_20170629062030
dipg0076_interval TUMOR
dipg0076_interval NORMAL
gg_mutation_report
ee
grc14378020_exome
grc14378018_exome
grc14378021_exome
grc14378019_exome
grc14378022_exome
family15 variants v3
i29p2-c-18094-iii
h1esc_mtesr1 samtools indel
test
v2649_v1_non-filtered_2017-07-24_10_39_21
v2649_v1_non-filtered_2017-07-24_10_39_21
62393865_s40 mvar 62393865_S40.FREEBAYES
62393865_s40 mvar 62393865_S40.GATK
62393865_s40 mvar 62393865_S40.SAMTOOLS
cmi
ppox
ppox
nextera4_03 03 2017_brca_13_s13_v5
hg001_grch37_giab_highconf_cg-illfb-illgatkhc-ion-10x-solid_chrom1-x_v 3 3 2_highconf_pgandrtgphasetransfer
tsc_27 01 2017_8_s8_v7
tsc_27 01 2017_8_s8_v7
cmt4
larissa_s11
myexome-1
c002_attactcg-tatagcct srt mkdups flt
c003_attactcg-atagaggc srt mkdups flt
c005_attactcg-cctatcct srt mkdups flt
final-ma145
mpe115_v1112
pep_0060
gordonsepilepsy filtered 2076
gordonsepilepsy filtered 2077
gordonsepilepsy filtered 2484
gordonsepilepsy filtered 2486
gordonsepilepsy filtered 2487_pool
gordonsepilepsy normalized 2076
gordonsepilepsy normalized 2077
gordonsepilepsy normalized 2484
gordonsepilepsy normalized 2486
gordonsepilepsy normalized 2487_pool
outputvcforig-sve05k
12ac02301-1_s1 genome
13ac00301-2_s1 genome
15ac02301_s1 genome
15ac02302_s1 genome
15ac02302_s1 genome
15ac02303_s1 genome
2-ac-cap17_s1 genome
15ac02301_s1 genome
15ac02303_s1 genome
15ac02303_s1 genome
16hpc01701_s1 genome
16hpc01702_s1 genome
16hpc01703_s1 genome
15a02301_s1 genome
09pla02101_s1 genome
zehra_acar_variant_analysis_report-2
genome_adam_cuomo_v4_full_20170809151438
sl85 samtools snp
gpp10314_20120828021333_nucseek
gpp10315_20120828021333_nucseek
genome_none_none_v4_full_20170814115900 Aug
genome_none_none_v4_full_20170814115900 14
genome_none_none_v4_full_20170814115900 11:59:00
genome_none_none_v4_full_20170814115900 2017
variant_list
l-322-filtered-snps-indels
16on271_ionxpress_012
eb408_unique
eb409_unique
myexome-1 annotated mendelmd
myexome-1 annotated mendelmd
idash_ishimaki
idp34_annotado
combined sample_100.variant
combined sample_38.variant2
combined sample_39.variant3
combined sample_40.variant4
combined sample_41.variant5
combined sample_42.variant6
combined sample_43.variant7
combined sample_44.variant8
combined sample_45.variant9
combined sample_46.variant10
combined sample_47.variant11
combined sample_48.variant12
combined sample_49.variant13
combined sample_50.variant14
combined sample_51.variant15
combined sample_53.variant16
combined sample_54.variant17
combined sample_55.variant18
combined sample_56.variant19
combined sample_57.variant20
combined sample_59.variant21
combined sample_60.variant22
combined sample_61.variant23
combined sample_62.variant24
combined sample_63.variant25
combined sample_64.variant26
combined sample_66.variant27
combined sample_67.variant28
combined sample_68.variant29
combined sample_69.variant30
combined sample_70.variant31
combined sample_71.variant32
combined sample_72.variant33
combined sample_73.variant34
combined sample_74.variant35
combined sample_91.variant36
combined sample_92.variant37
combined sample_93.variant38
combined sample_94.variant39
combined sample_95.variant40
combined sample_96.variant41
combined sample_97.variant42
combined sample_98.variant43
combined sample_99.variant44
mt2379_s1
fyc5
dna-data-2017-08-27
isabela
g104-1_bowtie2_dupremoved_realigned_v0 1 19mpileup_dummy
anemia
a_kheyri final
pytbv dbsnpa
1445140
46651510241455_annotated
mm170802ap
an035_hg19
allfamilies AWI
allfamilies AWJ
allfamilies AWK
allfamilies AWL
allfamilies AWM
allfamilies BIR
allfamilies BQ0
allfamilies BIP
allfamilies BIQ
fam3 AWI
fam3 AWJ
fam3 AWK
n498_snp_indel_anno
sample13_s1_s1_001_filtered_dp10_splitted
sample14_s2_s2_001_filtered_dp10_splitted
sample15_s3_s3_001_filtered_dp10_splitted
p0085_filtered
variants
refseq_hg38_cds merged symbol igv-capture hist coverage
chu17257-cha-zoe_s2
full_genome
15071143293692125889425
1507114365681-1642853908
genome_tim_dotson_v5_full_20171008065907
genesmarker
mitovcf_file
snps raw-snps 17_0233
snps raw-snps 17_0234
snps raw-snps 17_0235
62408779_s7 mvar 62408779_S7.FREEBAYES
62408779_s7 mvar
62408779_s7 mvar 62408779_S7.GATK
62408779_s7 mvar 62408779_S7.SAMTOOLS
genome_christian_muller_v3_full_20161102032233
genome_christian_muller_v3_full_20161102032233
genome_christian_muller_v3_full_20171011070154 Oct
genome_christian_muller_v3_full_20171011070154 11
genome_christian_muller_v3_full_20171011070154 07:01:54
genome_christian_muller_v3_full_20171011070154 2017
ashksample HG002
ashksample HG003
ashksample HG004
mpileup-final_calls_32716
ioncode_0105_fn25 bam-25 IonCode_0105_FN25.bam
ioncode_0105_fn25 bam-25 [25]
ioncode_0105_fn25 bam-25 (single)
ioncode_0105_fn25 bam-25 (Reads,
ioncode_0105_fn25 bam-25 Locally
ioncode_0105_fn25 bam-25 Realigned,
ioncode_0105_fn25 bam-25 Variants,
ioncode_0105_fn25 bam-25 EXON,
ioncode_0105_fn25 bam-25 AAC,
ioncode_0105_fn25 bam-25 AIFOG)
17-11096s1 germline-multisample gatk annotated 17-11096s1
17-11096s1 germline-multisample gatk annotated 17-11097s2
17-11096s1 germline-multisample gatk annotated 17-11098s1
17-11096s1 germline-multisample gatk annotated 17-11099s1
dossier4-di450-2-b00h4r3_hg19_snp annot
r_2016_06_15_14_03_10_user_mx-267-exomess_pool37_5b552 570 872
5500xl_23312002_2013_06_25_exomas16_2h495 processed recal
5500xl_23312002_2013_06_25_exomas16_2h496 processed recal
ca
snps raw-variants selected
snps raw
71161510240931_annotated-4
fakhrieh_salemi gatk snp
fakhrieh_salemi gatk snp
index31
fakhrieh_salemi gatk indel
filter output step3
chh6738_annovar
82937_v1
5840_s17
5516_s23
75_filt_10x
15001702300578a snp-1
qw2315_combined_r1 fastq raw
62388010_s7 mvar 62388010_S7.FREEBAYES
62388010_s7 mvar 62388010_S7.GATK
62388010_s7 mvar 62388010_S7.SAMTOOLS
eb1954_unique
f1 H02H9ALXX_1_F01_K0512P_Human_NoIndex_2-25348_Spuler_Lab_R1
f1 (paired)
f1 trimmed
f1 (paired)
f1 (Reads)
f1 -
f1 locally
f1 realigned
f1 (Variants,
f1 AAC)
allllllllllllyblswd
pdb336 vep
pdb346 vep
327_c879tanxx_gatagaca_l005 bam filtered vep Protein_position
327_c879tanxx_gatagaca_l005 bam filtered vep Amino_acids
327_c879tanxx_gatagaca_l005 bam filtered vep Codons
327_c879tanxx_gatagaca_l005 bam filtered vep Existing_variation
327_c879tanxx_gatagaca_l005 bam filtered vep Extra
339_c879tanxx_aaggacac_l005 bam filtered vep Protein_position
327_c879tanxx_gatagaca_l005 bam filtered vep Protein_position
pg_merged_chr19 recode PG1
339_c879tanxx_aaggacac_l005 bam filtered vep Amino_acids
327_c879tanxx_gatagaca_l005 bam filtered vep Amino_acids
327_c879tanxx_gatagaca_l005 bam filtered vep Codons
339_c879tanxx_aaggacac_l005 bam filtered vep Codons
339_c879tanxx_aaggacac_l005 bam filtered vep Existing_variation
327_c879tanxx_gatagaca_l005 bam filtered vep Existing_variation
327_c879tanxx_gatagaca_l005 bam filtered vep Extra
339_c879tanxx_aaggacac_l005 bam filtered vep Extra
pg_merged_chr19 recode PG2
pg_merged_chr19 recode PG3
pg_merged_chr19 recode PG4
tz1
tz1
wes_0001 hg19 bwa gatk freebayes combined
fam5 cleaned 3403_16
fam5 cleaned 3404_16
fam5 cleaned 3405_16
fam5 cleaned 3422_16
variants default
variants default
variants default
variants default
cds 3403_16
cds 3404_16
cds 3405_16
cds 3422_16
snps raw-variants selected 3403_16
snps raw-variants selected 3404_16
snps raw-variants selected 3405_16
snps raw-variants selected 3422_16
tsvc_variants_ionxpress_032
24_genetics_snv_99 8 slt
b12
1528098
damold_variant
damold_variant
tumor_sample brca
t30541_annotated_calls
t30541_annotated_calls
tumor_sample brca
nipe_alignment snps
halo_cad_march_17
halo_cad_march_17
mm170835gc
mm171122md
261_emreatak_v1_non-filtered_2016-09-01_06_25_23
upload2ensembl
snps raw MG15-000
snps raw MG15-001
snps raw MG15-002
snps raw SHA-06-33146
watson
sg5_onco_2_s2_v13
rawdata23andme
fam001 NG171210431
fam001 NG171210432
fam001 NG171210433
tsc_7_5_s5_v13
5_s5
5_s5 genome
trio_parsed_vcf15_03359procol_vcf_report overall_15_03359procol_R1_converted_Unique_Output.pjt
trio_parsed_vcf15_03359procol_vcf_report 15_06810matcol
trio_parsed_vcf15_03359procol_vcf_report 15_06811patcol
na12878 recessive
ex-15004
fpd-aix-mes-312-12
fpd-alg-mad-1230-3
jg31048rm_filtered-jrmeena-copy 117543
5517_sorted_hg19
example_snp
er-447_an6 ann hg38_multianno_umd
na12878 compound_heterozygous
552117_ngs_ex
552017_ngs_ex
552217_ngs_ex
annotation final
552217_ngs_ex annotated mendelmd
miller
abdullah_h_mahmood_ngs_032_17 ionxpress_011 r_2017_11_03_08_01_58_user_s5-0138-35-copy_of_ngs_032_17_aip_48_ornek_2
mm180101la
mm180104ea
mm180106mm
mm180110lp
mm180111m
mm180112f
1_s1 genome
1_s1
1_s1
2_s2
3_s3
4_s4
hboc12
10049_haplotypecaller_target
hgcat_input_example-3
child2_indexed
ptc-wgs combined vep gnomad
dels
d233
cpt10
33011510240923_annotated
amal-report-2
073_tsvc_variants
046_tsvc_variants
045_tsvc_variants
044_tsvc_variants
043_tsvc_variants
042_tsvc_variants
033_tsvc_variants
031_tsvc_variants
030_tsvc_variants
sm006-1 both
sm007-1 both
sm008-1 both
55001703319634a raw
01pjhc5_s1_l001_r0trimunpaired_cut_fastqc
01pex6c4_s1_indel_filter_end
mm180211ms
aml-1726_v1_non-filtered_2017-02-26_03_51_07
gt_so_4086_igt_1r
index13_otb1697_gerard goyette_500-049a_human_hex_av5-utr_50x_03232016 deduplicated realigned recalibrated snpeff snpsift
index9_otb1693_gerard goyette_500-049a_human_hex_av5-utr_50x_03232016 deduplicated realigned recalibrated snpeff snpsift
index34_otb3338_gerard goyette_500-049a-2_human_hex_av5-utr_50x_06112016 deduplicated realigned recalibrated snpeff snpsift
18063
21_s21
nist_integratedcalls_12datasets_130517_hethomvarpass_vqsrv2 15
21_s21 genome
gfg_filtered_unphased_genotypes_vcf
schinzel_giedion
432 varscan snp snpann
mng17-30918-p-lin003-patient-0001-e9504_mutation_report1
n2_s17
tsvc_variants_ionxpress_001
tsvc_variants_ionxpress_004
lanjinglingc2017103103501 mkdup sorted genotypegvcf
mmg003343
hodakb10_snp_indel_anno
hodakb12_snp_indel_anno
hodakt10_snp_indel_anno
hodakt12_snp_indel_anno
patient ann filtered
62334902_s25-161111_k00359_0038_bhg532bbxx-normal-illuwes-4f0ca40f-mvar
62334902_s25-161111_k00359_0038_bhg532bbxx-normal-illuwes-4f0ca40f-mvar
mp91583 both
ancestrydna
el-exome_s1
tsvc_variants_ionxpress_001-5225
9040 snpeff high
9040 cleaned_snpindel
9040 snpeff moderate
ex_013_mod
94533-0209701724_ms_onbait
promethease-1
71161510240931_annotated-4
hsp116-ii-1-filtered_variants
annovar hg19_multianno_pass
miller snpeff
s308
s315_9
248419675_annotated
test
variants
tsvc_variants_ionxpress_002-4
tsvc_variants_ionxpress_002-4
annotation final
ex
ex-sf
tsvc_variants_ionxpress_040
ap253-3 final
aaa
acacia
filtered
scz009_trimmed samtools
dnl109758_dez imputed
output 09_chr1 fa filtered3
45655-cr-ensemble
galaxy103-varscan_on_data_102
test
m1_rms1_10
m1_rms1_1
m1_rms1_11
m1_rms1_12
m1_rms1_14
m1_rms1_15
m1_rms1_13
m1_rms1_16
m1_rms1_17
m1_rms1_18
m1_rms1_19
m1_rms1_3
m1_rms1_2
m1_rms1_5
m1_rms1_4
m1_rms1_6
m1_rms1_7
m1_rms1_8
m1_rms1_9
mm180725at
mm180706dm
img-20181008-wa0006
tcga-bf-a1pu-01a-11d-a19a-08
pbrpl18h2_-_sravanthi_filtered_2018-09-27_04_08_32
breast1 1
sample1
mo-mi-abdi1130 final
u697_bwa_picard
164649418_s1 ann select dbsnp
na12877-rep1_s1
na12877-rep1_s1
f txt
f
2-fl-ha_482-01
miller
ctr0100487_mex076_alain_mancinas_201814015100_pass
bra19324freebayes
traning-sample-vcf-file
lapatrada pol indel
22603_s43
22603_s55
ns1-6
ns1-5 final
ns2-5 filtered variants
ns2-10 final
ns4-4
ns4-5
ns4-6
sama-karam_s1
copy-of-pof-ii-1-filtered-snps-indels-query output genome_summary
hsp108-ii-1-filtered_variants
2636_s28
2761_s29
4450_s11
6306_s1
6343_s27
6422_s23
6424_s25
6426_s21
12016_s26
12030_s5
12061_s9
12066_s20
12067_s13
12068_s19
12078_s17
12083_s14
12086_s22
12092_s33
12107_s6
16420_s8
16431_s7
16441_s18
17503_s31
17507_s32
2632_s12
sy-51_s2
sy-52_s3
2632_s12
2632_s12
jp5186_chip
32
na12878 dominant
miller
filtered_merged_a00k
rm-274 final
pm-286 final
diu946-001_results_diu946-001 final
shr
genome_jeffrey_bloom_v5_full_20190110052330
genome_jeffrey_bloom_v5_full_20190110052330
ht12d final
gatk f008 reheader
father
sec-2-18-7_filtered
sample_file
wanguard_s1
cdh6-52
full_combined_excel
miller
my var-final
62455815_s29 mvar
tsvc_variants_ionxpress_002
59876-as-ensemble
59876-as-ensemble
rf3717
56001801068581a snp
56001801066395a snp
56001801066395a indel
fmsd_filtered_snp_indel
180919fr-013-1
tsvc_variants_ioncode_0249
37-g0191 raw_variants
mr
mr
wes 6160 filtered recode
1886106_bak chr20
genome_susan_abernathy_v4_full_20190218171918
drift-nimh_freeze2_brmenn
9etks0122_annotation
17on508_ioncode_0113
a-full_variant_table
gm12878
hd829_190221_nb551050_0207_ahvwygbgx9 germline
solo_-a-star-wars-story-trailer
ctr0100514_mex083_jonathan_resendiz_20190502090400_pass
ctr0100502_mex079_amisaday_mora_20190330015800
200567_mutation_report1_filtered
qmul_trio_lof_assignment_2019
sample_hardfiltered
trio2 snpeff canon annotated exons dhg21091-v
trio2 snpeff canon annotated exons dhg21610-v
trio2 snpeff canon annotated exons dhg21611-v
8wkyncwo
8wkyncwo
mm160117hb v200
skaz004 gatk snp
porto_final_annot intervar_annovar
53586-full_variant_table
53586-full_variant_table
dna-data-2019-03-03
60820188484921_wgz snp-4
gi-variants-passed-homoz
wes_0012 hg38
rcl1126
wt108005 snp
wt108005fu0 snp
wt108005mu0 snp
mm190528hvp
mm190623opd
myexome
54871510242650_annotated-2
aghdas_dehghani qualified
plink
filtered4
filtered2
filtered5
filtered6
mpileup-final_calls_arg_046
111
p001_fim
xah
2_s2
kemikp79
h8m mutect2
001 final
60820188472738 snp
allsamples as snp_indel_pass_annotated
h7 indel_final
h11 snp_final
ashwath_ramji_slb567__wes_annotated_vcf
60820188484090 snp
56001808052608_wgz sv
f70
mr50 2
60820188481224 snp
60820188481224 indel1
yushu_s1 hg19_multianno
lh-2005601_umi hg19_multianno
pcg-f60 allchr snpeff p sal sal10_1 clinvar candidate_genes_tagged
genom_v5_full_20190304173844
144336383-full
144336383-full
moss final
62421900_s18-180124_k00541_0065_bhnjl7bbxx-normal-illuwesagi-76f236ce-freb filt pass
mmcs-209a
trio 2010_06 ychr sites-v2
trio 2010_06 ychr sites-v2
trio 2010_06 ychr sites-v2
file
tsvc_variants_ionxpress_006
f204-1528-proband
f204-1533-proband2
f204-1533-proband2
f204-1533-proband2
cp00040635 filtered indel
cp00040635 filtered snp
s216 g
6-na1287 both
00126 vep
demo1
60820188477917 filtered snp
f000043987_dp5_tag
2019_09_14t01_36_55z_suma_ionxpress_003
azm002
19508-01-01_s2
mm005
bm011
193810-bpl33-fg3374-sal-pi-19-16-4228-rhamppcr2_s123_l001_q20l30_sorted_primtv_snps
dg001 final
83356 33710_s2 smcounter anno
07-ms_s7 filtered vt snps indels annotated hg19_multianno
08-dh_s8 filtered vt snps indels annotated hg19_multianno
09-gf_s9 filtered vt snps indels annotated hg19_multianno
06t10508_snvintersect
95t14234_snvintersect
hht25
60820188482844 cnv
galaxy4-vcfselectsamples__on_data_1
62644690_s62 hpcl fboth pass
62644690_s62 bcfc filt pass
drift-nimh snps indels vqsr qced
62644690_s62 hpcl fboth pass
62644690_s62 bcfc filt pass
chan_pitt final
leila somatic
43_s43
44_s44
30_s30
nunez_a-2
variants selected
variants selected
liw
liw
nba852-001 variants
selected variants chr6
selected variants chr6
1351s
1352s
1353s
genome_aaron_hill_v3_full_20191101162607
skeletal
vqsr_snp_indel hc recaled
out
fomiga
94310feb
94410feb
718
chnaka
udp2568_axeq_1_hs37d5_remdup-uniqmap
udp5436_axeq_1_hs37d5_remdup-uniqmap
udp2569_axeq_1_hs37d5_remdup-uniqmap
udp2570_axeq_1_hs37d5_remdup-uniqmap
udp5435_axeq_1_hs37d5_remdup-uniqmap
udp2568_axeq_1_hs37d5_remdup-uniqmap
udp5436_axeq_1_hs37d5_remdup-uniqmap
udp2569_axeq_1_hs37d5_remdup-uniqmap
udp2570_axeq_1_hs37d5_remdup-uniqmap
sleepdisorders_saxena_sleep_exome_
funcotator_output
pjgl final
s75952_filtered_snps_and_indels
s75952_filtered_snps_and_indels
gen_coords_2546da25
gen_coords_4297ccf5
gen_coords_e4ad64d7
gen_coords_2546da25
gen_coords_2a24f493
20191018_null_jozsefpocsai_1_vcf
alves-daniel
ibg-2-cgm-0130 final
20041952_fiebersyndrome
axiomgt1 calls
136
914
914
dk31-akp-run025
wes413_annotated hg19_multianno
20159-01-01_s13-kopie
20160-01-01_s14-kopie
20160-02-01_s15-kopie
20161-01-01_s16-kopie
20162-01-01_s17-kopie
20163-01-01_s18-kopie
20165-01-01_s19-kopie
20166-01-01_s20-kopie
20167-01-01_s21-kopie
20168-01-01_s22-kopie
sano-converted-xao3oovlc7fnhcwi
60820188481023_wgz sv
nb26r3b7-vcf
nb26r3b7
nb26r3b7-vcf
ca-full_variant_table
df-full_variant_table
il-full_variant_table
le-full_variant_table
p767-full_variant_table
pa883-full_variant_table
p545-full_variant_table
p38bis-full_variant_table
2-pd
15_s15
17_s17
18_s18
mm200519jpm
mm200520lff
002-64854-300-scex
vep
haplotypecaller normalized sort
60820188477428 filtered snp
metin-yusa-ezelsoy
tsonexp104
na12878 recessive
f06400088-ib-ex-60-1639-mahdi-papolzaee-x_s46 soft_filtered
1jzxjfqlmt6b6sjn
sg8_171109_m03874_0051_000000000-bc4b6_osteo_7_s7_v13
2388
2388_2
mm200704jip pass
mm200801fps
mm200802avc
mm200803lca
pa_1_filt_10x
pa_2_filt_10x
pa_2_filt_10x
pa_3_filt_10x
pa_4_filt_10x
tsvc_variants_ionxpress_032
tsvc_variants_ionxpress_029
tsvc_variants_ionxpress_028
tsvc_variants_ionxpress_027
christinas-dna-raw-data
christinas-dna-raw-data
f06400419-ib-ex-34-1651-narges-nikzad-x-7d5-orion-ilya-1_s17 soft_filtered-1
257_mg_v1
ancestrydna
h06400150-ib-ex-60-1801-aliasghar-faghan-tonaj-x soft_filtered
g06400841-ib-ex-60-1790-lia-amanlo-x_s18 soft_filtered
h06400082-ib-ex-60-1795_s23 soft_filtered
g06400842-ib-ex-60-1791_s19 soft_filtered
h06400150-ib-ex-60-1801-aliasghar-faghan-tonaj-x soft_filtered
rbna2s annoted
mm200818ekc pass
60820188476706_wgz snp
60820188477428 filtered snp
60820188477428 filtered indel
mt9975_s20b_raw_onlyvariants
nb4y474q
chr1_tb
chrx_tb
f06400088-ib-ex-60-1639-mahdi-papolzaee-x_s46 soft_filtered
62716307_s105-200325_a00853_0090_bhnncndmxx-normal-illuwestwist-c50063e5-mvar
56001801068832b_wgz indel
56001801068832b_wgz snp
i06400152-ib-ex-60-1844-ehsan-ilya-biotech-orion-raw-data-9-ilya-biotech-4_s237 soft_filtered
data_trios
child filtered_variants
father filtered_variants
mother filtered_variants
raha-nazari
i06401043-ib-ex-60-1962-parsa-riazi-ilya-biotech-100x-7d5-4_s155 soft_filtered
2039528
cypcyp_20170119
lf7070
4k20002_01 gatk
myheritage_raw_dna_data
inbound8305150685853676453
42171
42440
94231510241520_annotated
lscsousa-37862-convertido
db-142035-19648
62792253_s65 bcfc filt pass
li29247
dnl435773_hfn
mm2
genome_benjamin_beeler_v5_full_20201120080226
genome_benjamin_beeler_v5_full_20201120080226
mn1_1_dkdn200006670-1a_hhwwtdsxy_filt_10x
dnaroberta
vcf2
s2421nr2_snvs
2020-005022-full_variant_table
k06401019-ib-ex-60-2014-fateme-pour-orion-raw-data-ilya-biotech_s3 soft_filtered
1351s
1352s
1353s
1352s
1351s
dnl415328_mwu
premaidha_pandita
8_s8
casescomb_anno_nochr vep
controlcomb_anno_vep
013 final
013 final
a1 mutect somatic snv mm10_multianno
a2 mutect somatic snv mm10_multianno
a3 mutect somatic snv mm10_multianno
a4 mutect somatic snv mm10_multianno
a5 mutect somatic snv mm10_multianno
mm210202rsv
mm210206egs
mm210202rsv
example-4 1-bnd
55101705103716_annotated
15001711234580a snp
merged_pe_ann-1
galaxy43-snpeff_eff__on_data_37
60820188472777 cnv
xyk885-001
galaxy6-vcffilter__3022nr6
galaxy6-vcffilter_3022nr4
galaxy7-vcffilter_3022nr8
galaxy7-vcffilter__3022nr7
galaxy36-vcffilter__3466nr4
galaxy7-vcffilter__3466nr40
a
hocanf12689796 cnvnator filter reheader
schinzel_giedion
galaxy7-vcffilter__3466nr3
galaxy7-vcffilter__3466nr4
galaxy7-vcffilter__3466nr40
galaxy7-vcffilter__3466nr42
dados_brutos_saude
dna
20tes0779_fb
frasc37
15001711232689a snp
04-cn_s4
etb21-ktww
genome
wes08-paw final
10200154963-unkown-ib-ex-60-2156-amirreza-safavi-orion-raw-data-9d375-1_s67 soft_filtered
ng11yhb2uc
104001164731-unkownib-ex-60-2253ariyaeskandari-orion-rawdata-9d5-2_s86 soft_filtered
smallvariants filtered
m21 14_15b68a
file
dados_brutos_saude
galaxy8-vcffilter_3910nr1
c1-bcemep2073 snp indel excludeflt grch38
p1-bcemep2058 snp indel excludeflt grch38
c1-bcemep2073 snp indel excludeflt grch38
p1-bcemep2058 snp indel excludeflt grch38
ngs_variants
sample202111_ merge
fls_f1
fls_f1
abdelali_rgd43_1_s22_qualfilter2
89896
mm210618mmm
mm210618mmm
1_1-200000_1234n
62466786_s45 mvar
62466786_s45 mvar
filter output step1
468f2at-raw_hg19
dados_brutos_saude
snp_m4n4
ztc634-001 cnv grch38
ztc634-001 variants grch38
riya_final_variants
rajesh_father_final_variants
riya_sister_final_variants
sweety_das_mother_final_variants
hervkucsc final_compsc12
hervkucsc final_compsc13
hervkucsc final_compsc15
hervkucsc final_compsc16
hervkucsc final_compsc17
hervkucsc final_compsc18
hervkucsc final_compsc21
hervkucsc final_compsc22
hervkucsc final_compsc23
hervkucsc final_compsc24
hervkucsc final_compsc25
hervkucsc final_compsc26
hervkucsc final_compsc27
hervkucsc final_compsc28
hervkucsc final_compsc29
hervkucsc final_compsc30
hervkucsc final_compsc8
hervkucsc final_compsc10
hervkucsc final_compsc11
hervkucsc final_compsc9
hervkucsc final_compsc7
hervkucsc final_compsc2
hervkucsc final_compsc4
hervkucsc final_comp31
haplotypecaller_300_21
sl476778 qc recode
mm210921mll
vcffilter4321nr2
vcffilter4321nr1
c82258b6-cab8-419f-9847-26d3cb04de6c
gowrish_ghosh_7071491
lmivty4833qdq7qw
mk265 final
mk264 final
mk266 final
mk268 final
mk267 final
mm211102rsf
srr8898194
pai-convertido
genera-pai-dados-brutos
23andme
patient
lofreq1-annotation
meu-dna-convertido-v5
f83-1371_s1
f83-980_s1
f83-981_s1
test
test
15001710502500a snp
15001710502500a indel
tw-001-300447370701 hard-filtered
tw-001-300447370801 hard-filtered
tw-001-300447370901 hard-filtered
tw-001-300447371001 hard-filtered
pfeiffer-singleton
igb85_p_baserecal_precalread_varcall g
garrettgeminiuc-ng1kmmceb1-30x-wgs-sequencing_com-10-12-21 mito
eticket_ven014_12191851_1
wes018-ban final
wild final
15001711234580a snp
galaxy396-snpeff_eff__on_data_20_and_data_390
galaxy413-snpeff_eff__on_data_20_and_data_412
test
vars_mtec_s13
readme
153751
tm-001-300470609201_sample-4 hard-filtered
multisample final
all annotation 21
148225_eymennacar_93_final
sec5
galaxy13-vcffilter__on_data_11
myheritage_raw_dna_data
genome_kristen_hiser_v5_full_202204271056061
1ng1gd5leyg-1
output
output
documento-de-eunice
tm-001-300484487501-r1 hard-filtered
tm-001-300484487601 hard-filtered
ngs-5_s2
tw-001-300447371501 hard-filtered
tw-001-300458116301 hard-filtered-2
tm-001-300484487801 hard-filtered
mn1_1_dkdn200006670-1a_hhwwtdsxy_filt_10x
mn1_1_dkdn200006670-1a_hhwwtdsxy_filt_10x
bac931-001 variants grch38_
my_protein_filter_vep
drr006760 haplotypecaller
s65_cosmic_annovar hg38_multianno hg38_multianno
s96_cosmic_annovar hg38_multianno hg38_multianno
hsm03
paolo_maccallini_snp
paolo_maccallini_indel
tomkooy-ng1k4katmj-30x-wgs-sequencing_com-09-09-22 snp-indel genome
15001710502500a snp
na12878 compound_heterozygous
na12878 compound_heterozygous
na12878 compound_heterozygous
kemik154
2765 filtered indel
2765 filtered snp
rawdataoriginal
upj-1_annotation
gen1
63084816_s277 hpcl fboth pass
dados_brutos_423_saude
dados_brutos-fer_212_saude
liblalt53_variants funcotatedb37
ng1hpy2syw1
s_25_17 haplotypecaller filtered
damb121 variants
galaxy94-snpeff_eff__dt-sc1_filtered___100
test
test
variants_1132761_1003714
exome_tobias_qualls_7875dc_e9i96r
epf23-lugp final
mk266 final
mk265 final
mk264 final
mk268 final
mk267 final
freebayes-on-259-variants
br_2009 hard-filtered
88_1_4113063-4113122_fullgenome
88_1_4113063-4113122_fullgenome
sis-3299335378-52-a3-0222-full_variant_table
1-ng10uyr74p-30x-wgs-sequencing_com-01-16-24 snp-indel genome
leftfiltered
leftfiltered
wd_h final
lis_hg19 filt
62951226_s22 bcfc filt pass
62951226_s22 bcfc filt pass
63239608_s186 hpcl fboth pass_2
anotado
EXCLUDE SNP LIST:
EXCLUDE GROUPS:
3029
3030
test
LG_GGB_20171101
EXCLUDE SAVED GENE LIST:
93 genes
A
A
Ataxia
Atypical Hemolytic-Uremic Syndrome
CGH_AR
Childhood Renal panel
chronic nephrotic
CK
comprehensive kidny
Comprehensive Neuromuscular Disorders Panel
Congenital Disorders of Glycosylation Panel
Deb
DEB.ING
Dermatology Gene Panel
Diabetes
Ehler D
Epidermolysis Bullosa 2
Epidermolysis Bullosa Panel
epilepsy
Facial Dysostosis Panel
fanconi
Genes Got Time
HLA
HUS
Hypokalemia and Related Disorders Panel
Ichthyosis
ichthyosis2
ichthyosis3
immunodeficincy
jr
mayoclinic PN
metabolic
Mody
musclat dystrophy
Nada autosomal ressicev
nephrolithiasis
Nephrotic
Neurofibromatosis
Neuropathies
Neuropathies2
Neuropathies 3
ostiopetrosis
perxosomal
primary immunodef
Retinal Dystrophy
SEMD2
Skin and Connective Tissue Disorders Panel
SMED
Spastic Paraplegia
Spinal Muscular Atrophy
Stickler
thrompocytopenia
Treacher Collins syndrome
Treacher Collins syndrome2
white matter disorder
EXCLUDE GENE LIST:
SELECT INHERITANCE:
RECESSIVE HOMOZYGOUS
RECESSIVE COMPOUND HETEROZYGOUS
DOMINANT HETEROZYGOUS
X-LINKED RECESSIVE HEMIZYGOUS
X-LINKED DOMINANT HETEROZYGOUS
SELECT YOUR DISEASES:
OMIM:
Adams-Oliver syndrome 5, 616028 (3)
Adams-Oliver syndrome 6, 616589 (3)
Adenine phosphoribosyltransferase deficiency, 614723 (3)
Adenocarcinoma of lung, response to tyrosine kinase inhibitor in, 211980 (3)
Adenocarcinoma of lung, somatic, 211980 (3)
Adenocarcinoma of lung, somatic, 211980 (3)
Adenocarcinoma of lung, somatic, 211980 (3)
Adenocarcinoma, colonic, somatic (3)
Adenoma, periampullary, somatic (3)
Adenomas, multiple colorectal, 608456 (3)
Adenomas, salivary gland pleomorphic, somatic, 181030 (3)
Adenomatous polyposis coli, 175100 (3)
Adenosine deaminase deficiency, partial, 102700 (3)
Adenosine triphosphate, elevated, of erythrocytes, 102900 (3)
Adenylosuccinase deficiency, 103050 (3)
Adermatoglyphia, 136000 (3)
Adiponectin deficiency, 612556 (3)
Adrenal adenoma, somatic (3)
Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency, 202010 (3)
Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency, 201910 (3)
Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency, 201810 (3)
Adrenal hypoplasia, congenital, 300200 (3)
Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, 613743 (3)
Adrenocortical insufficiency, 612964 (3)
Adrenocortical tumor, somatic, (3)
Adrenocorticotropic hormone deficiency, 201400 (3)
Adrenoleukodystrophy, 300100 (3)
Adrenomyeloneuropathy, adult, 300100 (3)
Adult i phenotype without cataract, 110800 (3)
Advanced sleep phase syndrome, familial, 1, 604348 (3)
Advanced sleep-phase syndrome, familial, 2, 615224 (3)
Afibrinogenemia, congenital, 202400 (3)
Afibrinogenemia, congenital, 202400 (3)
Factor V and factor VIII, combined deficiency of, 613625 (3)
Factor V deficiency, 227400 (3)
Factor VII deficiency, 227500 (3)
Factor X deficiency, 227600 (3)
Factor XI deficiency, autosomal dominant, 612416 (3)
Factor XI deficiency, autosomal recessive, 612416 (3)
Factor XII deficiency, 234000 (3)
Factor XIIIA deficiency, 613225 (3)
Factor XIIIB deficiency, 613235 (3)
Failure of tooth eruption, primary, 125350 (3)
Familial Mediterranean fever, AD, 134610 (3)
Familial Mediterranean fever, AR, 249100 (3)
Familial adenomatous polyposis 3, 616415 (3)
Familial adenomatous polyposis 4, 617100 (3)
Familial cold autoinflammatory syndrome 2, 611762 (3)
Familial cold autoinflammatory syndrome 3, 614468 (3)
Familial cold inflammatory syndrome 1, 120100 (3)
Fanconi anemia, complementation group A, 227650 (3)
{Esophagitis, eosinophilic, 1} (2)
{Esophagitis, eosinophilic, 2} (2)
{Essential tremor, hereditary, 1}, 190300 (3)
{Exfoliation syndrome, susceptibility to}, 177650 (3)
{Fatty liver disease, nonalcoholic, susceptibility to, 1} (2)
{Fatty liver disease, nonalcoholic, susceptibility to, 2} (2)
{Fibrocalculous pancreatic diabetes, susceptibility to}, 608189 (3)
{Follicular lymphoma, susceptibility to, 1} (2)
{Gallbladder disease 4}, 611465 (3)
Afibrinogenemia, congenital, 202400 (3)
Agammaglobulinemia 1, 601495 (3)
Agammaglobulinemia 2, 613500 (3)
Agammaglobulinemia 3, 613501 (3)
Agammaglobulinemia 6, 612692 (3)
Agammaglobulinemia 8, autosomal dominant, 616941 (3)
Agammaglobulinemia, X-linked 1, 300755 (3)
Agammaglobulinemia, X-linked 2 (2)
Agenesis of the corpus callosum with peripheral neuropathy, 218000 (3)
Agnathia-otocephaly complex, 202650 (3)
Aicardi syndrome (2)
Aicardi-Goutieres syndrome 1, dominant and recessive, 225750 (3)
Aicardi-Goutieres syndrome 2, 610181 (3)
Aicardi-Goutieres syndrome 3, 610329 (3)
Aicardi-Goutieres syndrome 4, 610333 (3)
Aicardi-Goutieres syndrome 5, 612952 (3)
Aicardi-Goutieres syndrome 6, 615010 (3)
Aicardi-Goutieres syndrome 7, 615846 (3)
Al Kaissi syndrome, 617694 (3)
Al-Raqad syndrome, 616459 (3)
Alacrima, achalasia, and mental retardation syndrome, 615510 (3)
Alagille syndrome 1, 118450 (3)
Alagille syndrome 2, 610205 (3)
Aland Island eye disease, 300600 (3)
Alazami syndrome, 615071 (3)
Alazami-Yuan syndrome, 617126 (3)
Albinism, brown oculocutaneous, 203200 (3)
Albinism, oculocutaneous, type IA, 203100 (3)
Albinism, oculocutaneous, type IB, 606952 (3)
Albinism, oculocutaneous, type II, 203200 (3)
Albinism, oculocutaneous, type III, 203290 (3)
Albinism, oculocutaneous, type IV, 606574 (3)
Albinism, oculocutaneous, type V (2)
Albinism, oculocutaneous, type VI, 113750 (3)
Fanconi anemia, complementation group B, 300514 (3)
Fanconi anemia, complementation group C, 227645 (3)
Fanconi anemia, complementation group D1, 605724 (3)
Fanconi anemia, complementation group D2, 227646 (3)
Fanconi anemia, complementation group E, 600901 (3)
Fanconi anemia, complementation group F, 603467 (3)
Fanconi anemia, complementation group G, 614082 (3)
Fanconi anemia, complementation group I, 609053 (3)
Fanconi anemia, complementation group J, 609054 (3)
Fanconi anemia, complementation group L, 614083 (3)
Fanconi anemia, complementation group N, 610832 (3)
Fanconi anemia, complementation group O, 613390 (3)
Fanconi anemia, complementation group P, 613951 (3)
Fanconi anemia, complementation group Q, 615272 (3)
Fanconi anemia, complementation group S, 617883 (3)
{Gastric cancer risk after H. pylori infection}, 137215 (3)
{Gastric cancer risk after H. pylori infection}, 137215 (3)
{Gene expression, variation in, QTL} (2)
{Gene expression, variation in, QTL} (2)
{Gilles de la Tourette syndrome, susceptibility to}, 137580 (3)
{Glaucoma, normal tension, susceptibility to}, 606657 (3)
{Glaucoma, normal tension, susceptibility to}, 606657 (3)
{Glioblastoma 3}, 613029 (3)
{Glioma susceptibility 1}, 137800 (3)
Albinism, oculocutaneous, type VII, 615179 (3)
Albinism-deafness syndrome (2)
Alcohol sensitivity, acute, 610251 (3)
Aldosterone to renin ratio raised (3)
Aldosteronism, glucocorticoid-remediable, 103900 (3)
Alexander disease, 203450 (3)
Alkaptonuria, 203500 (3)
Alkuraya-Kucinskas syndrome, 617822 (3)
Allan-Herndon-Dudley syndrome, 300523 (3)
Alopecia areata 1 (2)
Alopecia areata 2 (2)
Alopecia universalis, 203655 (3)
Alopecia, androgenetic, 1 (2)
Alopecia, androgenetic, 2 (2)
Alopecia, androgenetic, 3 (2)
Alopecia-mental retardation syndrome 1 (2)
Alopecia-mental retardation syndrome 2 (2)
Alopecia-mental retardation syndrome 3 (2)
Alpha-1-antichymotrypsin deficiency (3)
Alpha-2-macroglobulin deficiency, 614036 (1)
Alpha-2-plasmin inhibitor deficiency, 262850 (3)
Alpha-fetoprotein deficiency, 615969 (3)
Alpha-ketoglutarate dehydrogenase deficiency, 203740 (1)
Alpha-methylacetoacetic aciduria, 203750 (3)
Alpha-methylacyl-CoA racemase deficiency, 614307 (3)
Alpha-thalassemia myelodysplasia syndrome, somatic, 300448 (3)
Alpha-thalassemia/mental retardation syndrome, 301040 (3)
Alpha-thalassemia/mental retardation syndrome, type 1 (4)
Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity, 609889 (3)
Alport syndrome 1, X-linked, 301050 (3)
Alport syndrome 2, autosomal recessive, 203780 (3)
Alport syndrome 2, autosomal recessive, 203780 (3)
Alport syndrome 3, autosomal dominant, 104200 (3)
Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis (4)
Alstrom syndrome, 203800 (3)
Alternating hemiplegia of childhood 1, 104290 (3)
Fanconi anemia, complementation group T, 616435 (3)
Fanconi renotubular syndrome 1 (2)
Fanconi renotubular syndrome 4, with maturity-onset diabetes of the young, 616026 (3)
Fanconi-Bickel syndrome, 227810 (3)
Farber lipogranulomatosis, 228000 (3)
Fascioscapulohumeral muscular dystrophy 2, digenic, 158901 (3)
Fatty liver, acute, of pregnancy, 609016 (3)
Febrile seizures, familial, 1 (2)
Febrile seizures, familial, 10 (2)
Febrile seizures, familial, 11, 614418 (3)
Febrile seizures, familial, 2 (2)
Febrile seizures, familial, 3A, 604403 (3)
Febrile seizures, familial, 3B, 613863 (3)
Febrile seizures, familial, 5 (2)
Febrile seizures, familial, 6 (2)
Febrile seizures, familial, 7 (2)
Febrile seizures, familial, 8, 611277 (3)
Febrile seizures, familial, 9 (2)
{Glioma susceptibility 2}, 613028 (3)
{Glioma susceptibility 4} (2)
{Glioma susceptibility 5} (2)
{Glioma susceptibility 6} (2)
{Glioma susceptibility 7} (2)
{Glioma susceptibility 8} (2)
{Glioma susceptibility 9}, 616568 (3)
{Glioma, susceptibility to, somatic}, 137800 (3)
{Glomerulosclerosis, focal segmental, 4, susceptibility to}, 612551 (3)
?Craniofacioskeletal syndrome (2)
Alternating hemiplegia of childhood 2, 614820 (3)
Alveolar capillary dysplasia with misalignment of pulmonary veins, 265380 (3)
Alveolar soft-part sarcoma, 606243 (3)
Alzheimer disease 1, familial, 104300 (3)
Alzheimer disease 17 (2)
Alzheimer disease 6 (2)
Alzheimer disease 8 (2)
Alzheimer disease, type 3, 607822 (3)
Alzheimer disease, type 3, with spastic paraparesis and apraxia, 607822 (3)
Alzheimer disease, type 3, with spastic paraparesis and unusual plaques, 607822 (3)
Alzheimer disease-10 (2)
Alzheimer disease-11 (2)
Alzheimer disease-2, 104310 (3)
Alzheimer disease-4, 606889 (3)
Alzheimer disease-5 (2)
Alzheimer disease-7 (2)
Amelogenesis imperfecta, hypomaturation type, IIA6, 617217 (3)
Amelogenesis imperfecta, type 1E, 301200 (3)
Amelogenesis imperfecta, type IA, 104530 (3)
Amelogenesis imperfecta, type IB, 104500 (3)
Amelogenesis imperfecta, type IC, 204650 (3)
Amelogenesis imperfecta, type IF, 616270 (3)
Amelogenesis imperfecta, type IG (enamel-renal syndrome), 204690 (3)
Amelogenesis imperfecta, type IH, 616221 (3)
Amelogenesis imperfecta, type IIA1, 204700 (3)
Amelogenesis imperfecta, type IIA2, 612529 (3)
Amelogenesis imperfecta, type IIA3, 613211 (3)
Amelogenesis imperfecta, type IIA4, 614832 (3)
Amelogenesis imperfecta, type IIA5, 615887 (3)
Amelogenesis imperfecta, type IIIA, 130900 (3)
Amelogenesis imperfecta, type IJ, 617297 (3)
Amelogenesis imperfecta, type IV, 104510 (3)
Aminoacylase 1 deficiency, 609924 (3)
Amyloidosis, 3 or more types, 105200 (3)
Amyloidosis, Finnish type, 105120 (3)
Amyloidosis, familial visceral, 105200 (3)
Feingold syndrome 1, 164280 (3)
Feingold syndrome 2, 614326 (3)
Fetal akinesia deformation sequence, 208150 (3)
Fetal akinesia deformation sequence, 208150 (3)
Fetal hemoglobin quantitative trait locus 1, 141749 (3)
Fetal hemoglobin quantitative trait locus 1, 141749 (3)
Fetal hemoglobin quantitative trait locus 2 (2)
Fetal hemoglobin quantitative trait locus 3 (2)
Fetal hemoglobin quantitative trait locus 4 (2)
Fibrochondrogenesis 1, 228520 (3)
Fibrochondrogenesis 2, 614524 (3)
Fibrodysplasia ossificans progressiva, 135100 (3)
Fibromatosis, gingival, 2 (2)
Fibromatosis, gingival, 3 (2)
Fibromatosis, gingival, 4 (2)
Fibromatosis, gingival, 5, 617626 (3)
Fibrosis of extraocular muscles, congenital, 1, 135700 (3)
{Glucocorticoid therapy, response to}, 614400 (3)
{Gout susceptibility 4}, 612671 (3)
{Graft-versus-host disease, protection against}, 614395 (3)
{Graves disease, susceptibility to, 1} (2)
{Graves disease, susceptibility to, 2} (2)
{Graves disease, susceptibility to, X-linked} (2)
{H. pylori infection, susceptibility to}, 600263 (3)
{HDL response to hormone replacement, augmented} (3)
{HFE hemochromatosis, modifier of}, 235200 (3)
Amyloidosis, hereditary, transthyretin-related, 105210 (3)
Amyloidosis, primary localized cutaneous, 1, 105250 (3)
Amyloidosis, primary localized cutaneous, 3, 617920 (3)
Amyloidosis, renal, 105200 (3)
Amyotrophic lateral sclerosis 1, 105400 (3)
Amyotrophic lateral sclerosis 10, with or without FTD, 612069 (3)
Amyotrophic lateral sclerosis 11, 612577 (3)
Amyotrophic lateral sclerosis 12, 613435 (3)
Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia, 613954 (3)
Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, 300857 (3)
Amyotrophic lateral sclerosis 17, 614696 (3)
Amyotrophic lateral sclerosis 18, 614808 (3)
Amyotrophic lateral sclerosis 19, 615515 (3)
Amyotrophic lateral sclerosis 2, juvenile, 205100 (3)
Amyotrophic lateral sclerosis 20, 615426 (3)
Amyotrophic lateral sclerosis 21, 606070 (3)
Amyotrophic lateral sclerosis 22 with or without frontotemporal dementia, 616208 (3)
Amyotrophic lateral sclerosis 3 (2)
Amyotrophic lateral sclerosis 4, juvenile, 602433 (3)
Amyotrophic lateral sclerosis 5, juvenile, 602099 (3)
Amyotrophic lateral sclerosis 6, with or without frontotemporal dementia, 608030 (3)
Amyotrophic lateral sclerosis 7 (2)
Amyotrophic lateral sclerosis 8, 608627 (3)
Amyotrophic lateral sclerosis 9, 611895 (3)
Amyotrophy, hereditary neuralgic, 162100 (3)
Amytrophic lateral sclerosis 23, 617839 (3)
Analbuminemia, 616000 (3)
Anauxetic dysplasia 1, 607095 (3)
Anauxetic dysplasia 2, 617396 (3)
Andersen syndrome, 170390 (3)
Androgen insensitivity, 300068 (3)
Androgen insensitivity, partial, with or without breast cancer, 312300 (3)
Fibrosis of extraocular muscles, congenital, 2, 602078 (3)
Fibrosis of extraocular muscles, congenital, 3A, 600638 (3)
Fibrosis of extraocular muscles, congenital, 3B, 135700 (3)
Fibrosis of extraocular muscles, congenital, 3C (2)
Fibrosis of extraocular muscles, congenital, 5, 616219 (3)
Filippi syndrome, 272440 (3)
Fish-eye disease, 136120 (3)
Fletcher factor (prekallikrein) deficiency, 612423 (3)
Floating-Harbor syndrome, 136140 (3)
Focal cortical dysplasia, type II, somatic, 607341 (3)
Focal cortical dysplasia, type II, somatic, 607341 (3)
Focal dermal hypoplasia, 305600 (3)
Focal facial dermal dysplasia 3, Setleis type, 227260 (3)
Focal facial dermal dysplasia 4, 614974 (3)
Focal segmental glomerulosclerosis 8, 616032 (3)
Focal segmental glomerulosclerosis 9, 616220 (3)
{HIV infection, resistance to}, 609423 (2)
{HIV infection, susceptibility/resistance to} (3)
{HIV infection, susceptibility/resistance to} (3)
{HIV type 1, susceptibility to}, 609423 (3)
{HIV-1 disease, delayed progression of} (3)
{HIV-1 disease, rapid progression of} (3)
{HIV-1 viremia, susceptibility to}, 609423 (3)
{HIV-1, resistance to}, 609423 (3)
{HIV-1, susceptibility to}, 609423 (3)
Anemia, X-linked, with/without neutropenia and/or platelet abnormalities, 300835 (3)
Anemia, hemolytic, Rh-null, regulator type, 268150 (3)
Anemia, hemolytic, due to UMPH1 deficiency, 266120 (3)
Anemia, hypochromic microcytic, with iron overload 1, 206100 (3)
Anemia, neonatal hemolytic, fatal or near-fatal, 617948 (3)
Anemia, sideroblastic, 1, 300751 (3)
Bardet-Biedl syndrome 13, 615990 (3)
CINCA syndrome, 607115 (3)
CK syndrome, 300831 (3)
CLAPO syndrome, somatic, 613089 (3)
CLOVE syndrome, somatic, 612918 (3)
COACH syndrome, 216360 (3)
COACH syndrome, 216360 (3)
COACH syndrome, 216360 (3)
CODAS syndrome, 600373 (3)
COMMAD syndrome, 617306 (3)
COPD, rate of decline of lung function in, 606963 (3)
CPT II deficiency, infantile, 600649 (3)
CPT II deficiency, lethal neonatal, 608836 (3)
CPT II deficiency, myopathic, stress-induced, 255110 (3)
CPT deficiency, hepatic, type IA, 255120 (3)
CR1 deficiency (1)
CRASH syndrome, 303350 (3)
Caffey disease, 114000 (3)
Calcification of joints and arteries, 211800 (3)
Campomelic dysplasia with autosomal sex reversal, 114290 (3)
Campomelic dysplasia, 114290 (3)
Camptodactyly 1 (2)
Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, 208250 (3)
Camurati-Engelmann disease, 131300 (3)
Canavan disease, 271900 (3)
Candidiasis, familial, 1, autosomal dominant (2)
Candidiasis, familial, 2, autosomal recessive, 212050 (3)
Candidiasis, familial, 3 (2)
Folate malabsorption, hereditary, 229050 (3)
Fontaine progeroid syndrome, 612289 (3)
Forebrain defects (3)
Forsythe-Wakeling syndrome (2)
Foveal hypoplasia 1, 136520 (3)
Foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis, 609218 (3)
Fragile X syndrome, 300624 (3)
Fragile X tremor/ataxia syndrome, 300623 (3)
Frank-ter Haar syndrome, 249420 (3)
Fraser syndrome 1, 219000 (3)
Fraser syndrome 2, 617666 (3)
Fraser syndrome 3, 617667 (3)
Frasier syndrome, 136680 (3)
Frias syndrome (4)
Friedreich ataxia 2 (2)
Friedreich ataxia with retained reflexes, 229300 (3)
Friedreich ataxia, 229300 (3)
Frontometaphyseal dysplasia 1, 305620 (3)
{HIV/AIDS, susceptibility to}, 609423 (3)
{HIV1 infection, resistance to}, 609423 (3)
{HIV1, resistance to}, 609423 (3)
{Hangover, susceptibility to}, 610251 (3)
{Hashimoto thyroiditis}, 140300 (3)
{Hemangioma, capillary infantile, susceptibility to}, 602089 (3)
{Hemolytic uremic syndrome, atypical, susceptibility to, 1}, 235400 (3)
{Hemolytic uremic syndrome, atypical, susceptibility to, 2}, 612922 (3)
?Cutaneous telangiectasia and cancer syndrome, familial, 614564 (3)
Anemia, sideroblastic, 2, pyridoxine-refractory, 205950 (3)
Anemia, sideroblastic, 3, pyridoxine-refractory, 616860 (3)
Anemia, sideroblastic, 4, 182170 (3)
Anemia, sideroblastic, with ataxia, 301310 (3)
Aneurysm, intracranial berry, 1 (2)
Aneurysm, intracranial berry, 11 (2)
Aneurysm, intracranial berry, 2 (2)
Aneurysm, intracranial berry, 3 (2)
Aneurysm, intracranial berry, 4 (2)
Aneurysm, intracranial berry, 5 (2)
Aneurysm, intracranial berry, 7 (2)
Aneurysm, intracranial berry, 8 (2)
Aneurysmal bone cysts (2)
Angelman syndrome, 105830 (3)
Angio serpiginosum (2)
Angioedema, hereditary, type III, 610618 (3)
Angioedema, hereditary, types I and II, 106100 (3)
Angiofibroma, somatic (3)
Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps, 611773 (3)
Aniridia, 106210 (3)
Anisomastia (2)
Anonychia congenita, 206800 (3)
Anosmia, isolated congenital (2)
Anterior segment anomalies with or without cataract, 602588 (3)
Anterior segment dysgenesis 1, multiple subtypes, 107250 (3)
Anterior segment dysgenesis 2, multiple subtypes, 610256 (3)
Anterior segment dysgenesis 3, multiple subtypes, 601631 (3)
Anterior segment dysgenesis 4, 137600 (3)
Anterior segment dysgenesis 5, multiple subtypes, 604229 (3)
Anterior segment dysgenesis 6, multiple subtypes, 617315 (3)
Anterior segment dysgenesis 7, with sclerocornea, 269400 (3)
Anterior segment dysgenesis 8, 617319 (3)
Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis, 201750 (3)
Frontometaphyseal dysplasia 2, 617137 (3)
Frontonasal dysplasia 1, 136760 (3)
Frontonasal dysplasia 2, 613451 (3)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 1, 105550 (3)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2, 615911 (3)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 3, 616437 (3)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 4, 616439 (3)
Frontotemporal lobar degeneration with ubiquitin-positive inclusions, 607485 (3)
Frontotemporal lobar degeneration, TARDBP-related, 612069 (3)
Fructose intolerance, hereditary, 229600 (3)
Fructose-1,6-bisphosphatase deficiency, 229700 (3)
Fucosidosis, 230000 (3)
Fucosyltransferase 6 deficiency, 613852 (3)
Fuhrmann syndrome, 228930 (3)
Fumarase deficiency, 606812 (3)
Fundus albipunctatus, 136880 (3)
Fundus albipunctatus, 136880 (3)
{Hemolytic uremic syndrome, atypical, susceptibility to, 3}, 612923 (3)
{Hemolytic uremic syndrome, atypical, susceptibility to, 4}, 612924 (3)
{Hemolytic uremic syndrome, atypical, susceptibility to, 5}, 612925 (3)
{Hemolytic uremic syndrome, atypical, susceptibility to, 6}, 612926 (3)
{Hemolytic uremic syndrome, atypical, susceptibility to, 7}, 615008 (3)
{Hemolytic uremic syndrome, atypical, susceptibility to}, 235400 (3)
{Hemolytic uremic syndrome, atypical, susceptibility to}, 235400 (3)
?SERKAL syndrome, 611812 (3)
Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis, 207410 (3)
Aortic aneurysm, familial abdominal 1 (2)
Aortic aneurysm, familial abdominal 2 (2)
Aortic aneurysm, familial abdominal, 4 (2)
Aortic aneurysm, familial thoracic 1 (2)
Aortic aneurysm, familial thoracic 10, 617168 (3)
Aortic aneurysm, familial thoracic 2 (2)
Aortic aneurysm, familial thoracic 4, 132900 (3)
Aortic aneurysm, familial thoracic 6, 611788 (3)
Aortic aneurysm, familial thoracic 7, 613780 (3)
Aortic aneurysm, familial thoracic 8, 615436 (3)
Aortic aneurysm, familial thoracic 9, 616166 (3)
Aortic valve disease 1, 109730 (3)
Aortic valve disease 2, 614823 (3)
Apert syndrome, 101200 (3)
Aphasia, primary progressive, 607485 (3)
Aplasia of lacrimal and salivary glands, 180920 (3)
Aplastic anemia, 609135 (3)
Aplastic anemia, 609135 (3)
ApoA-I and apoC-III deficiency, combined (3)
Apolipoprotein A-II deficiency (3)
Apolipoprotein C-III deficiency, 614028 (3)
Apparent mineralocorticoid excess, 218030 (3)
Argininemia, 207800 (3)
Argininosuccinic aciduria, 207900 (3)
Aromatase deficiency, 613546 (3)
Aromatase excess syndrome, 139300 (3)
Aromatic L-amino acid decarboxylase deficiency, 608643 (3)
Arrhythmogenic right ventricular dysplasia 1, 107970 (3)
Arrhythmogenic right ventricular dysplasia 10, 610193 (3)
Arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair, 610476 (3)
Arrhythmogenic right ventricular dysplasia 11, 610476 (3)
Arrhythmogenic right ventricular dysplasia 12, 611528 (3)
Arrhythmogenic right ventricular dysplasia 2, 600996 (3)
Arrhythmogenic right ventricular dysplasia 3 (2)
Fundus flavimaculatus, 248200 (3)
GABA-transaminase deficiency, 613163 (3)
GAPO syndrome, 230740 (3)
GLOW syndrome, somatic mosaic, 618272 (3)
GLUT1 deficiency syndrome 1, infantile onset, severe, 606777 (3)
GLUT1 deficiency syndrome 2, childhood onset, 612126 (3)
GM1-gangliosidosis, type I, 230500 (3)
GM1-gangliosidosis, type II, 230600 (3)
GM1-gangliosidosis, type III, 230650 (3)
GM2-gangliosidosis, AB variant, 272750 (3)
GM2-gangliosidosis, several forms, 272800 (3)
GRACILE syndrome, 603358 (3)
Gabriele-de Vries syndrome, 617557 (3)
Galactokinase deficiency with cataracts, 230200 (3)
Galactose epimerase deficiency, 230350 (3)
Galactosemia, 230400 (3)
Galactosialidosis, 256540 (3)
{Hemorrhage, intracerebral, susceptibility to}, 614519 (3)
{Hemorrhage, intracerebral, susceptibility to}, 614519 (3)
{Hepatic fibrosis susceptibility due to Schistosoma mansoni infection} (2)
{Hepatitis B virus infection, susceptibility to}, 610424 (3)
{Hepatitis B virus, susceptibility to}, 610424 (3)
{Hepatitis B virus, susceptibility to}, 610424 (3)
{Hepatitis C virus infection, response to therapy of}, 609532 (3)
Arrhythmogenic right ventricular dysplasia 4 (2)
Arrhythmogenic right ventricular dysplasia 5, 604400 (3)
Arrhythmogenic right ventricular dysplasia 6 (2)
Arrhythmogenic right ventricular dysplasia 8, 607450 (3)
Arrhythmogenic right ventricular dysplasia 9, 609040 (3)
Arrhythmogenic right ventricular dysplasia, familial, 13, 615616 (3)
Arterial calcification, generalized, of infancy, 1, 208000 (3)
Arterial calcification, generalized, of infancy, 2, 614473 (3)
Arterial tortuosity syndrome, 208050 (3)
Arteriovenous malformation of the brain, somatic, 108010 (3)
Arthrogryposis multiplex congenita, distal, type 1, 108120 (3)
Arthrogryposis multiplex congenita, distal, type 2B, 601680 (3)
Arthrogryposis multiplex congenita, neurogenic, with myelin defect, 617468 (3)
Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development, 618265 (3)
Arthrogryposis, distal, type 10 (2)
Arthrogryposis, distal, type 1B, 614335 (3)
Arthrogryposis, distal, type 2A, 193700 (3)
Arthrogryposis, distal, type 2B, 601680 (3)
Arthrogryposis, distal, type 2B, 601680 (3)
Arthrogryposis, distal, type 2B, 601680 (3)
Arthrogryposis, distal, type 3, 114300 (3)
Arthrogryposis, distal, type 5, 108145 (3)
Arthrogryposis, distal, type 5D, 615065 (3)
Arthrogryposis, distal, type 8, 178110 (3)
Arthrogryposis, distal, with impaired proprioception and touch, 617146 (3)
Arthrogryposis, renal dysfunction, and cholestasis 1, 208085 (3)
Arthrogryposis, renal dysfunction, and cholestasis 2, 613404 (3)
Arthropathy, progressive pseudorheumatoid, of childhood, 208230 (3)
Arts syndrome, 301835 (3)
Asparagine synthetase deficiency, 615574 (3)
Gallbladder disease 1, 600803 (3)
Gallbladder disease 2 (2)
Gallbladder disease 3 (2)
Galloway-Mowat syndrome 1, 251300 (3)
Galloway-Mowat syndrome 2, X-linked, 301006 (3)
Galloway-Mowat syndrome 3, 617729 (3)
Galloway-Mowat syndrome 4, 617730 (3)
Galloway-Mowat syndrome 5, 617731 (3)
Galloway-Mowat syndrome 6, 618347 (3)
Galloway-Mowat syndrome 7, 618348 (3)
Gardner syndrome, 175100 (3)
Gastric cancer, hereditary diffuse, with or without cleft lip and/or palate, 137215 (3)
Gastric cancer, somatic, 137215 (3)
Gastric cancer, somatic, 613659 (3)
Gastric cancer, somatic, 613659 (3)
Gastric cancer, somatic, 613659 (3)
Gastric cancer, somatic, 613659 (3)
Gastric cancer, somatic, 613659 (3)
{Hepatitis C virus, resistance to}, 609532 (3)
{Hepatitis C virus, response to therapy of}, 609532 (3)
{Hepatitis C virus, susceptibility to}, 609532 (3)
{High density lipoprotein cholesterol level QTL 7} (3)
{High density lipoprotein cholesterol, low serum, 3} (2)
{Hirschsprung disease, protection against}, 142623 (3)
{Hirschsprung disease, susceptibility to, 1}, 142623 (3)
{Hirschsprung disease, susceptibility to, 2}, 600155 (3)
?Deafness, X-linked 6, 300914 (3)
Aspartate aminotransferase, serum level of, QTL1, 614419 (3)
Aspartylglucosaminuria, 208400 (3)
Asplenia, isolated congenital, 271400 (3)
Asthma and nasal polyps, 208550 (3)
Ataxia with isolated vitamin E deficiency, 277460 (3)
Ataxia, cerebellar, Cayman type, 601238 (3)
Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia, 208920 (3)
Ataxia, posterior column, with retinitis pigmentosa, 609033 (3)
Ataxia, sensory, 1, autosomal dominant, 608984 (3)
Ataxia-oculomotor apraxia 3, 615217 (3)
Ataxia-oculomotor apraxia 4, 616267 (3)
Ataxia-pancytopenia syndrome, 159550 (3)
Ataxia-telangiectasia, 208900 (3)
Ataxia-telangiectasia-like disorder 1, 604391 (3)
Atelosteogenesis, type I, 108720 (3)
Atelosteogenesis, type II, 256050 (3)
Atelosteogenesis, type III, 108721 (3)
Athabaskan brainstem dysgenesis syndrome, 601536 (3)
Atransferrinemia, 209300 (3)
Atrial fibrillation, familial, 1 (2)
Atrial fibrillation, familial, 10, 614022 (3)
Atrial fibrillation, familial, 11, 614049 (3)
Atrial fibrillation, familial, 12, 614050 (3)
Atrial fibrillation, familial, 13, 615377 (3)
Atrial fibrillation, familial, 14, 615378 (3)
Atrial fibrillation, familial, 16, 613120 (3)
Atrial fibrillation, familial, 17, 611819 (3)
Atrial fibrillation, familial, 2 (2)
Atrial fibrillation, familial, 3, 607554 (3)
Atrial fibrillation, familial, 4, 611493 (3)
Atrial fibrillation, familial, 6, 612201 (3)
Atrial fibrillation, familial, 7, 612240 (3)
Atrial fibrillation, familial, 8 (2)
Atrial fibrillation, familial, 9, 613980 (3)
Gastric cancer, somatic, 613659 (3)
Gastric cancer, somatic, 613659 (3)
Gastric cancer, somatic, 613659 (3)
Gastroesophageal reflux (2)
Gastrointestinal defects and immunodeficiency syndrome, 243150 (3)
Gastrointestinal stromal tumor, 606764 (3)
Gastrointestinal stromal tumor, 606764 (3)
Gastrointestinal stromal tumor, familial, 606764 (3)
Gastrointestinal stromal tumor, somatic, 606764 (3)
Gastrointestinal ulceration, recurrent, with dysfunctional platelets, 618372 (3)
Gaucher disease, atypical, 610539 (3)
Gaucher disease, perinatal lethal, 608013 (3)
Gaucher disease, type I, 230800 (3)
Gaucher disease, type II, 230900 (3)
Gaucher disease, type III, 231000 (3)
Gaucher disease, type IIIC, 231005 (3)
Gaze palsy, familial horizontal, with progressive scoliosis, 1, 607313 (3)
{Hirschsprung disease, susceptibility to, 3}, 613711 (3)
{Hirschsprung disease, susceptibility to, 4}, 613712 (3)
{Hirschsprung disease, susceptibility to, 5} (2)
{Hirschsprung disease, susceptibility to, 6} (2)
{Hirschsprung disease, susceptibility to, 7} (2)
{Hirschsprung disease, susceptibility to, 8} (2)
{Hirschsprung disease, susceptibility to, 9} (2)
{Hodgkin disease susceptibility, pseudoautosomal} (2)
{Hodgkin lymphoma, susceptibility to}, 236000 (3)
Atrial septal defect 1 (2)
Atrial septal defect 2, 607941 (3)
Atrial septal defect 3, 614089 (3)
Atrial septal defect 4, 611363 (3)
Atrial septal defect 5, 612794 (3)
Atrial septal defect 6, 613087 (3)
Atrial septal defect 7, with or without AV conduction defects, 108900 (3)
Atrial septal defect 8, 614433 (3)
Atrial septal defect 9, 614475 (3)
Atrial standstill 2, 615745 (3)
Atrial standstill, digenic (GJA5/SCN5A), 108770 (3)
Atrichia with papular lesions, 209500 (3)
Atrioventricular septal defect 3, 600309 (3)
Atrioventricular septal defect 4, 614430 (3)
Atrioventricular septal defect 5, 614474 (3)
Atrioventricular septal defect, partial, with heterotaxy syndrome, 606217 (3)
Au-Kline syndrome, 616580 (3)
Auditory neuropathy and optic atrophy, 617717 (3)
Auditory neuropathy, autosomal dominant, 1, 609129 (3)
Auditory neuropathy, autosomal recessive, 1, 601071 (3)
Aural atresia, congenital, 607842 (3)
Auriculocondylar syndrome 1, 602483 (3)
Auriculocondylar syndrome 2, 614669 (3)
Auriculocondylar syndrome 3, 615706 (3)
Autoimmune disease, multisystem, infantile-onset, 1, 615952 (3)
Autoimmune disease, multisystem, infantile-onset, 2, 617006 (3)
Autoimmune disease, multisystem, with facial dysmorphism, 613385 (3)
Autoimmune lymphoproliferative syndrome, type IA, 601859 (3)
Autoimmune lymphoproliferative syndrome, type IB, 601859 (3)
Autoimmune lymphoproliferative syndrome, type II, 603909 (3)
Autoimmune lymphoproliferative syndrome, type III, 615559 (3)
Gaze palsy, familial horizontal, with progressive scoliosis, 2, 617542 (3)
Geleophysic dysplasia 1, 231050 (3)
Geleophysic dysplasia 2, 614185 (3)
Geleophysic dysplasia 3, 617809 (3)
Generalized epilepsy with febrile seizures plus, type 9, 616172 (3)
Geniospasm (2)
Genitopatellar syndrome, 606170 (3)
Germ cell tumors, somatic, 273300 (3)
Geroderma osteodysplasticum, 231070 (3)
Gerstmann-Straussler disease, 137440 (3)
Ghosal hematodiaphyseal syndrome, 231095 (3)
Giant axonal neuropathy-1, 256850 (3)
Giant platelet disorder, isolated, 231200 (3)
Gigantism due to GHRF hypersecretion (1)
Gillespie syndrome, 206700 (3)
Gillessen-Kaesbach-Nishimura syndrome, 263210 (3)
Gitelman syndrome, 263800 (3)
{Human herpesvirus 8, susceptibility to} (2)
{Hyperapobetalipoproteinemia, susceptibility to} (3)
{Hypercalciuria, absorptive, susceptibility to}, 143870 (3)
{Hypercholesterolemia, familial, due to LDLR defect, modifier of}, 143890 (3)
{Hypercholesterolemia, familial, modifier of}, 143890 (3)
{Hypercholesterolemia, familial, modifier of}, 143890 (3)
{Hypercholesterolemia, susceptibility to}, 143890 (3)
{Hypercholesterolemia, susceptibility to}, 143890 (3)
?Deafness, X-linked 7, 301018 (3)
Autoimmune lymphoproliferative syndrome, type V, 616100 (3)
Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia, 240300 (3)
Autoinflammation with arthritis and dyskeratosis, 617388 (3)
Autoinflammation with infantile enterocolitis, 616050 (3)
Autoinflammation, antibody deficiency, and immune dysregulation syndrome, 614878 (3)
Autoinflammation, panniculitis, and dermatosis syndrome, 617099 (3)
Autoinflammatory syndrome, familial, Behcet-like, 616744 (3)
Autonomic nervous system dysfunction (3)
Avascular necrosis of the femoral head, 608805 (3)
Axenfeld-Rieger syndrome, type 1, 180500 (3)
Axenfeld-Rieger syndrome, type 3, 602482 (3)
Ayme-Gripp syndrome, 601088 (3)
B-cell expansion with NFKB and T-cell anergy, 616452 (3)
B-cell non-Hodgkin lymphoma, high-grade (3)
Bainbridge-Ropers syndrome, 615485 (3)
Baker-Gordon syndrome, 618218 (3)
Baller-Gerold syndrome, 218600 (3)
Bamforth-Lazarus syndrome, 241850 (3)
Band heterotopia, 600348 (3)
Baraitser-Winter syndrome 1, 243310 (3)
Baraitser-Winter syndrome 2, 614583 (3)
Barber-Say syndrome, 209885 (3)
Bardet-Biedl syndrome 1, 209900 (3)
Bardet-Biedl syndrome 10, 615987 (3)
Bardet-Biedl syndrome 12, 615989 (3)
Bardet-Biedl syndrome 16, 615993 (3)
Bardet-Biedl syndrome 17, 615994 (3)
Bardet-Biedl syndrome 2, 615981 (3)
Bardet-Biedl syndrome 21, 617406 (3)
Bardet-Biedl syndrome 3, 600151 (3)
Bardet-Biedl syndrome 4, 615982 (3)
Bardet-Biedl syndrome 5, 615983 (3)
Bardet-Biedl syndrome 6, 605231 (3)
Glanzmann thrombasthenia, 273800 (3)
Glanzmann thrombasthenia, 273800 (3)
Glass syndrome, 612313 (3)
Glaucoma 1, open angle, 1O, 613100 (3)
Glaucoma 1, open angle, E, 137760 (3)
Glaucoma 1, open angle, F, 603383 (3)
Glaucoma 1, open angle, G, 609887 (3)
Glaucoma 1, open angle, H (2)
Glaucoma 1, open angle, I (2)
Glaucoma 1, open angle, M (2)
Glaucoma 1, open angle, N (2)
Glaucoma 1, open angle, P (4)
Glaucoma 1A, primary open angle, 137750 (3)
Glaucoma 1B, primary open angle, adult onset (2)
Glaucoma 1C, primary open angle (2)
Glaucoma 1D, primary open angle (2)
Glaucoma 1K, primary open angle, juvenile-onset (2)
Glaucoma 3, primary congenital, C (2)
Glaucoma 3, primary congenital, D, 613086 (3)
{Hyperlipidemia, familial combined, susceptibility to}, 602491 (3)
{Hypersensitivity syndrome, carbamazepine-induced, susceptibility to}, 608579 (3)
{Hypertension, diastolic, resistance to}, 608622 (3)
{Hypertension, essential, salt-sensitive}, 145500 (3)
{Hypertension, essential, susceptibility to, 1}, 145500 (2)
{Hypertension, essential, susceptibility to, 2}, 145500 (2)
{Hypertension, essential, susceptibility to, 3}, 145500 (2)
{Hypertension, essential, susceptibility to, 4}, 145500 (2)
Bardet-Biedl syndrome 7, 615984 (3)
Bardet-Biedl syndrome 8, 615985 (3)
Bardet-Biedl syndrome 9, 615986 (3)
Bare lymphocyte syndrome, type I, 604571 (3)
Bare lymphocyte syndrome, type I, 604571 (3)
Bare lymphocyte syndrome, type I, due to TAP2 deficiency, 604571 (3)
Bare lymphocyte syndrome, type II, complementation group A, 209920 (3)
Bare lymphocyte syndrome, type II, complementation group C, 209920 (3)
Bare lymphocyte syndrome, type II, complementation group D, 209920 (3)
Bare lymphocyte syndrome, type II, complementation group E, 209920 (3)
Barrett esophagus/esophageal adenocarcinoma, 614266 (3)
Barrett esophagus/esophageal adenocarcinoma, 614266 (3)
Barrett esophagus/esophageal adenocarcinoma, 614266 (3)
Bart-Pumphrey syndrome, 149200 (3)
Barth syndrome, 302060 (3)
Bartter syndrome, type 1, 601678 (3)
Bartter syndrome, type 2, 241200 (3)
Bartter syndrome, type 3, 607364 (3)
Bartter syndrome, type 4a, 602522 (3)
Bartter syndrome, type 4b, digenic, 613090 (3)
Bartter syndrome, type 4b, digenic, 613090 (3)
Bartter syndrome, type 5, antenatal, transient, 300971 (3)
Basal cell carcinoma, somatic, 605462 (3)
Basal cell carcinoma, somatic, 605462 (3)
Basal cell carcinoma, somatic, 605462 (3)
Basal cell carcinoma, somatic, 605462 (3)
Basal cell nevus syndrome, 109400 (3)
Basal cell nevus syndrome, 109400 (3)
Basal cell nevus syndrome, 109400 (3)
Basal ganglia calcification, idiopathic, 1, 213600 (3)
Basal ganglia calcification, idiopathic, 2 (2)
Basal ganglia calcification, idiopathic, 4, 615007 (3)
Basal ganglia calcification, idiopathic, 5, 615483 (3)
Basal ganglia calcification, idiopathic, 6, 616413 (3)
{Hypertension, essential, susceptibility to, 5}, 145500 (2)
Glaucoma 3, primary congenital, E, 617272 (3)
Glaucoma 3, primary infantile, B (2)
Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset, 231300 (3)
Glaucoma, primary open angle, juvenile-onset, 2 (2)