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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096805copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318 SNORA94, LIMD1-AS1, 120 more genes
    nsv7042236inversion1nstd229human GRCh38 chr3: 48,697,468-48,701,595 , GRCh37.p13 chr3: 48,734,901-48,739,028 IP6K2
    nsv6713527copy number variation1nstd229human GRCh38 chr3: 48,685,865-48,691,867 , GRCh37.p13 chr3: 48,723,298-48,729,300 IP6K2, NCKIPSD
    nsv6709142copy number variation1nstd229human GRCh38 chr3: 48,694,720-48,697,792 , GRCh37.p13 chr3: 48,732,153-48,735,225 IP6K2
    nsv6706836copy number variation1nstd229human GRCh38 chr3: 48,699,430-48,699,755 , GRCh37.p13 chr3: 48,736,863-48,737,188 IP6K2
    nsv6700836copy number variation1nstd229human GRCh38 chr3: 48,056,801-51,204,000 , GRCh37.p13 chr3: 48,098,291-51,241,431 APEH, SLC26A6, 129 more genes
    nsv6555273inversion1nstd223human GRCh38 chr3: 48,713,959-48,714,318 , GRCh37.p13 chr3: 48,751,392-48,751,751 IP6K2
    nsv6553171inversion1nstd223human GRCh38 chr3: 48,709,742-48,710,745 , GRCh37.p13 chr3: 48,747,175-48,748,178 IP6K2
    nsv6536436inversion1nstd223human GRCh38 chr3: 48,703,717-48,704,786 , GRCh37.p13 chr3: 48,741,150-48,742,219 IP6K2
    nsv6372055copy number variation1nstd223human GRCh38 chr3: 48,386,801-49,230,000 , GRCh37.p13 chr3: 48,428,291-49,267,433 NCKIPSD, UCN2, 44 more genes
    nsv6368484copy number variation1nstd223human GRCh38 chr3: 48,694,720-48,697,787 , GRCh37.p13 chr3: 48,732,153-48,735,220 IP6K2
    nsv6366869copy number variation1nstd223human GRCh38 chr3: 48,707,716-48,712,499 , GRCh37.p13 chr3: 48,745,149-48,749,932 IP6K2
    nsv6365306copy number variation1nstd223human GRCh38 chr3: 48,429,601-48,926,800 , GRCh37.p13 chr3: 48,471,010-48,964,233 PRKAR2A-AS1, SNORA94, 25 more genes
    nsv6315166copy number variation1nstd102humanPathogenic GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376 TMEM89, TGM4, 129 more genes
    nsv6253986mobile element insertion1nstd215human GRCh38 chr3: 48,708,611-48,708,611 , GRCh37.p13 chr3: 48,746,044-48,746,044 IP6K2
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv6079557insertion1nstd212human GRCh38 chr3: 48,708,602-48,708,602 , GRCh37.p13 chr3: 48,746,035-48,746,035 IP6K2
    nsv6069182insertion1nstd212human GRCh38 chr3: 48,708,398-48,708,398 , GRCh37.p13 chr3: 48,745,831-48,745,831 IP6K2
    nsv5993413copy number variation1nstd212human GRCh38 chr3: 48,714,267-48,714,340 , GRCh37.p13 chr3: 48,751,700-48,751,773 IP6K2
    nsv5959566insertion1nstd209human GRCh38 chr3: 48,708,597-48,708,597 , GRCh37.p13 chr3: 48,746,030-48,746,030 IP6K2
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