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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7077728inversion1nstd229human GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353 LOC283172, PPP1R10P1, 175 more genes
    nsv7070443inversion1nstd229human GRCh38 chr11: 125,887,512-126,792,902 , GRCh37.p13 chr11: 125,757,407-126,662,797 CDON, TIRAP, 21 more genes
    nsv6917381copy number variation1nstd229human GRCh38 chr11: 126,592,214-126,807,966 , GRCh37.p13 chr11: 126,462,109-126,677,861 LOC105369561, LOC101929427, 1 more genes
    nsv6913210copy number variation1nstd229human GRCh38 chr11: 126,655,366-126,660,652 , GRCh37.p13 chr11: 126,525,261-126,530,547 KIRREL3, LOC101929427
    nsv6911811copy number variation1nstd229human GRCh38 chr11: 126,652,562-126,653,843 , GRCh37.p13 chr11: 126,522,457-126,523,738 LOC101929427, KIRREL3
    nsv6905446copy number variation1nstd229human GRCh38 chr11: 126,595,206-126,917,742 , GRCh37.p13 chr11: 126,465,101-126,787,638 LOC105369561, LOC105369559, 2 more genes
    nsv6899705copy number variation1nstd229human GRCh38 chr11: 126,637,432-126,651,393 , GRCh37.p13 chr11: 126,507,327-126,521,288 LOC101929427, KIRREL3
    nsv6637558copy number variation1nstd102humanPathogenic GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576 OR8B8, LOC107984373, 234 more genes
    nsv6470339copy number variation1nstd223human GRCh38 chr11: 126,592,214-126,807,966 , GRCh37.p13 chr11: 126,462,109-126,677,861 KIRREL3, LOC105369561, 1 more genes
    nsv6459462copy number variation1nstd223human GRCh38 chr11: 126,651,572-128,129,487 , GRCh37.p13 chr11: 126,521,467-127,999,382 KIRREL3-AS2, LINC02712, 16 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6291396copy number variation1nstd102humanUncertain significance GRCh37 chr11: 126,462,437-126,678,981 , GRCh38.p12 chr11: 126,592,542-126,809,086 LOC105369561, LOC101929427, 1 more genes
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv6132082copy number variation1nstd213human GRCh37 chr11: 126,220,000-126,870,001 , GRCh38.p12 chr11: 126,350,105-127,000,105 MIR3167, KIRREL3-AS2, 8 more genes
    nsv6098827insertion1nstd212human GRCh38 chr11: 126,668,745-126,668,745 , GRCh37.p13 chr11: 126,538,640-126,538,640 KIRREL3, LOC101929427
    nsv5333424translocation1nstd200human GRCh37 chr11: 126,520,789-126,520,789 , GRCh37 chr11: 126,520,688-126,520,688 , GRCh38.p12 chr11: 126,650,793-126,650,793 , GRCh38.p12 chr11: 126,650,894-126,650,894 LOC101929427, KIRREL3
    nsv4981209copy number variation1nstd200human GRCh38 chr11: 126,668,210-126,668,796 , GRCh37.p13 chr11: 126,538,105-126,538,691 KIRREL3, LOC101929427
    nsv4981208copy number variation1nstd200human GRCh38 chr11: 126,667,718-126,669,016 , GRCh37.p13 chr11: 126,537,613-126,538,911 KIRREL3, LOC101929427
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