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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6876648copy number variation1nstd229human GRCh38 chr9: 73,165,555-73,173,282 , GRCh37.p13 chr9: 75,780,471-75,788,198 ANXA1
    nsv6876635copy number variation1nstd229human GRCh38 chr9: 72,384,161-74,793,192 , GRCh37.p13 chr9: 74,999,077-77,408,108 LOC101927329, LOC100289351, 27 more genes
    nsv6874338copy number variation1nstd229human GRCh38 chr9: 73,144,601-73,212,500 , GRCh37.p13 chr9: 75,759,517-75,827,416 ANXA1
    nsv6867184copy number variation1nstd229human GRCh38 chr9: 72,981,725-73,370,430 , GRCh37.p13 chr9: 75,596,641-75,985,346 LOC105376081, LOC101927281, 3 more genes
    nsv6864363copy number variation1nstd229human GRCh38 chr9: 73,114,421-73,360,170 , GRCh37.p13 chr9: 75,729,337-75,975,086 LOC101927281, LOC105376082, 1 more genes
    nsv6863034copy number variation1nstd229human GRCh38 chr9: 72,906,209-73,538,839 , GRCh37.p13 chr9: 75,521,125-76,153,755 DPP3P2, LOC105376084, 7 more genes
    nsv6858598copy number variation1nstd229human GRCh38 chr9: 73,136,615-73,153,215 , GRCh37.p13 chr9: 75,751,531-75,768,131 ANXA1
    nsv6858263copy number variation1nstd229human GRCh38 chr9: 72,621,927-73,648,904 , GRCh37.p13 chr9: 75,236,843-76,263,820 RPS20P24, LINC01474, 13 more genes
    nsv6858203copy number variation1nstd229human GRCh38 chr9: 73,121,493-73,181,192 , GRCh37.p13 chr9: 75,736,409-75,796,108 ANXA1
    nsv6637502copy number variation1nstd102humanUncertain significance GRCh37 chr9: 70,966,262-76,901,382 , GRCh38.p12 chr9: 68,351,346-74,286,466 RPS20P24, MAMDC2-AS1, 77 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6455564copy number variation1nstd223human GRCh38 chr9: 73,148,601-73,150,400 , GRCh37.p13 chr9: 75,763,517-75,765,316 ANXA1
    nsv6455241copy number variation1nstd223human GRCh38 chr9: 73,165,501-73,171,900 , GRCh37.p13 chr9: 75,780,417-75,786,816 ANXA1
    nsv6453716copy number variation1nstd223human GRCh38 chr9: 72,906,209-73,538,841 , GRCh37.p13 chr9: 75,521,125-76,153,757 ANXA1, LOC105376084, 7 more genes
    nsv6446182copy number variation1nstd223human GRCh38 chr9: 73,154,901-73,156,500 , GRCh37.p13 chr9: 75,769,817-75,771,416 ANXA1
    nsv6445927copy number variation1nstd223human GRCh38 chr9: 73,149,601-73,151,100 , GRCh37.p13 chr9: 75,764,517-75,766,016 ANXA1
    nsv6445782copy number variation1nstd223human GRCh38 chr9: 73,167,055-73,167,425 , GRCh37.p13 chr9: 75,781,971-75,782,341 ANXA1
    nsv6441387copy number variation1nstd223human GRCh38 chr9: 73,158,455-73,160,886 , GRCh37.p13 chr9: 75,773,371-75,775,802 ANXA1
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
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