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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094164copy number variation1nstd102humanUncertain significance GRCh37 chr11: 26,353,823-26,681,991 , GRCh38.p12 chr11: 26,332,276-26,660,444 MUC15, LOC105376598, 2 more genes
    nsv7074285inversion1nstd229human GRCh38 chr11: 25,121,393-29,376,238 , GRCh37.p13 chr11: 25,142,939-29,397,785 RPL37AP7, LOC107984367, 40 more genes
    nsv7070460inversion1nstd229human GRCh38 chr11: 21,520,035-27,618,155 , GRCh37.p13 chr11: 21,541,581-27,639,702 RPS25P1, LOC105376598, 48 more genes
    nsv6915789copy number variation1nstd229human GRCh38 chr11: 26,450,601-26,583,400 , GRCh37.p13 chr11: 26,472,148-26,604,947 LOC107987160, ANO3, 1 more genes
    nsv6908106copy number variation1nstd229human GRCh38 chr11: 26,563,343-26,566,375 , GRCh37.p13 chr11: 26,584,890-26,587,922 ANO3, MUC15
    nsv6906158copy number variation1nstd229human GRCh38 chr11: 18,831,701-26,837,040 , GRCh37.p13 chr11: 18,853,248-26,858,587 HTATIP2, LINC02686, 68 more genes
    nsv6903355copy number variation1nstd229human GRCh38 chr11: 25,530,877-26,656,773 , GRCh37.p13 chr11: 25,552,423-26,678,320 LOC105376598, LOC107987160, 7 more genes
    nsv6902656copy number variation1nstd229human GRCh38 chr11: 25,900,269-26,725,298 , GRCh37.p13 chr11: 25,921,816-26,746,845 LOC100533706, LOC105376598, 6 more genes
    nsv6620843copy number variation1nstd224human GRCh37 chr11: 25,453,646-27,226,591 , GRCh38.p12 chr11: 25,432,100-27,205,044 BBOX1, BBOX1-AS1, 11 more genes
    nsv6442755copy number variation1nstd223human GRCh38 chr11: 26,560,521-26,561,178 , GRCh37.p13 chr11: 26,582,068-26,582,725 ANO3, MUC15
    nsv6438772copy number variation1nstd223human GRCh38 chr11: 26,567,892-26,568,429 , GRCh37.p13 chr11: 26,589,439-26,589,976 ANO3, MUC15
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6132359copy number variation1nstd213human GRCh37 chr11: 26,390,000-26,790,001 , GRCh38.p12 chr11: 26,368,453-26,768,454 ANO3, MUC15, 2 more genes
    nsv6039278copy number variation1nstd212human GRCh38 chr11: 26,564,718-26,564,771 , GRCh37.p13 chr11: 26,586,265-26,586,318 ANO3, MUC15
    nsv5978512insertion1nstd209human GRCh38 chr11: 26,564,789-26,564,789 , GRCh37.p13 chr11: 26,586,336-26,586,336 ANO3, MUC15
    nsv5713773mobile element insertion2nstd211human GRCh38 chr11: 26,560,153-26,560,153 , GRCh37.p13 chr11: 26,581,700-26,581,700 ANO3, MUC15
    nsv5551663insertion1nstd206human GRCh38 chr11: 26,564,725-26,564,789 , GRCh37.p13 chr11: 26,586,272-26,586,336 ANO3, MUC15
    nsv5404576mobile element insertion1nstd206human GRCh38 chr11: 26,560,153-26,560,204 , GRCh37.p13 chr11: 26,581,700-26,581,751 ANO3, MUC15
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
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