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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5927138copy number variation1nstd209human GRCh38 chr8: 143,260,698-143,260,756 , GRCh37.p13 chr8: 144,342,868-144,342,926 ZFP41
    nsv5633104insertion1nstd207human GRCh38 chr8: 143,260,132-143,260,132 , GRCh37.p13 chr8: 144,342,302-144,342,302 ZFP41
    nsv5632588insertion1nstd207human GRCh38 chr8: 143,261,940-143,261,940 , GRCh37.p13 chr8: 144,344,110-144,344,110 ZFP41
    nsv5627704insertion1nstd207human GRCh38 chr8: 143,252,778-143,252,778 , GRCh37.p13 chr8: 144,334,948-144,334,948 ZFP41
    nsv5579324copy number variation1nstd207human GRCh38 chr8: 143,255,781-143,255,848 , GRCh37.p13 chr8: 144,337,951-144,338,018 ZFP41
    nsv5575668copy number variation1nstd207human GRCh38 chr8: 143,261,831-143,261,929 , GRCh37.p13 chr8: 144,344,001-144,344,099 ZFP41
    nsv5372180translocation1nstd200human GRCh38 chr8: 143,260,418-143,260,418 , GRCh38 chr8: 143,259,975-143,259,975 , GRCh37.p13 chr8: 144,342,145-144,342,145 , GRCh37.p13 chr8: 144,342,588-144,342,588 ZFP41
    nsv5301183copy number variation1nstd204human GRCh38.p13 chr8: 143,160,494-143,803,360 , GRCh37.p13 chr8: 144,241,911-144,743,529 TIGD5, MAPK15, 36 more genes
    nsv5254948copy number variation1nstd204human GRCh38.p13 chr8: 143,167,001-143,860,200 , GRCh37.p13 chr8: 144,248,418-144,743,525 LOC105375798, LINC02990, 41 more genes
    nsv5253030copy number variation1nstd204human GRCh38.p13 chr8: 143,160,501-143,441,400 , GRCh37.p13 chr8: 144,241,918-144,523,570 MAFA-AS1, TOP1MT, 13 more genes
    nsv4742430copy number variation1nstd199human GRCh37 chr8: 144,343,995-144,344,095 , GRCh38.p12 chr8: 143,261,825-143,261,925 ZFP41
    nsv4740387copy number variation1nstd199human GRCh37 chr8: 144,338,164-144,338,369 , GRCh38.p12 chr8: 143,255,994-143,256,199 ZFP41
    nsv4729603copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 144,262,042-146,295,771 , GRCh38.p12 chr8: 143,180,625-145,070,385 CYC1, EEF1D, 112 more genes
    nsv4729040copy number variation1nstd102humanUncertain significance GRCh37 chr8: 144,285,728-144,534,781 , GRCh38.p12 chr8: 143,204,267-143,452,611 GPIHBP1, ZNF696, 11 more genes
    nsv4728931copy number variation1nstd102humanUncertain significance GRCh37 chr8: 144,111,911-144,384,136 , GRCh38.p12 chr8|NT_187573.1: 20,782-158,983 , GRCh38.p12 chr8: 143,030,494-143,301,966 RPS26P36, LOC102725000, 13 more genes
    nsv4676049copy number variation1nstd102humanPathogenic GRCh37 chr8: 143,616,831-144,930,611 , GRCh38.p12 chr8: 142,535,470-143,848,439 PYCR3, MROH4P, 69 more genes
    nsv4675692copy number variation1nstd102humanUncertain significance GRCh37 chr8: 143,570,920-144,459,613 , GRCh38.p12 chr8: 142,489,559-143,377,443 SLURP2, THEM6, 37 more genes
    nsv4675664copy number variation1nstd102humanPathogenic GRCh37 chr8: 128,877,995-146,295,771 , GRCh38.p12 chr8: 127,865,749-145,070,385 LOC105375789, LINC02990, 270 more genes
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 TOP1MT, SLA, 379 more genes
    nsv4675029copy number variation1nstd102humanPathogenic GRCh37 chr8: 142,132,678-145,569,441 , GRCh38.p12 chr8: 141,122,579-144,345,779 RHPN1-AS1, MIR6847, 117 more genes
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