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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093770copy number variation1nstd102humanUncertain significance GRCh37 chr11: 59,939,307-60,235,941 , GRCh38.p12 chr11: 60,171,834-60,468,468 MS4A5, MS4A4E, 7 more genes
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv6913935copy number variation1nstd229human GRCh38 chr11: 60,283,291-60,459,015 , GRCh37.p13 chr11: 60,050,764-60,226,488 MS4A7, MS4A5, 4 more genes
    nsv6912860copy number variation1nstd229human GRCh38 chr11: 60,442,062-60,475,690 , GRCh37.p13 chr11: 60,209,535-60,243,163 MS4A5, MS4A1
    nsv6908615copy number variation1nstd229human GRCh38 chr11: 60,427,371-60,434,872 , GRCh37.p13 chr11: 60,194,844-60,202,345 MS4A5
    nsv6908366copy number variation1nstd229human GRCh38 chr11: 60,121,080-60,521,495 , GRCh37.p13 chr11: 59,888,553-60,288,968 MS4A5, MS4A4E, 10 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6905193copy number variation1nstd229human GRCh38 chr11: 60,442,101-60,442,178 , GRCh37.p13 chr11: 60,209,574-60,209,651 MS4A5
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6902899copy number variation1nstd229human GRCh38 chr11: 60,433,403-60,433,612 , GRCh37.p13 chr11: 60,200,876-60,201,085 MS4A5
    nsv6899815copy number variation1nstd229human GRCh38 chr11: 60,421,201-60,429,111 , GRCh37.p13 chr11: 60,188,674-60,196,584 MS4A5
    nsv6621007copy number variation1nstd224human GRCh37 chr11: 60,128,004-60,491,092 , GRCh38.p12 chr11: 60,360,531-60,723,619 MS4A19P, MS4A5, 9 more genes
    nsv6475142copy number variation1nstd223human GRCh38 chr11: 60,437,001-60,556,000 , GRCh37.p13 chr11: 60,204,474-60,323,473 MS4A12, MS4A5, 2 more genes
    nsv6473218copy number variation1nstd223human GRCh38 chr11: 60,432,587-60,442,995 , GRCh37.p13 chr11: 60,200,060-60,210,468 MS4A5
    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
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6286030insertion1nstd214human GRCh38 chr11: 60,447,056-60,447,056 , GRCh37.p13 chr11: 60,214,529-60,214,529 MS4A5
    nsv6131998inversion1nstd213human GRCh37 chr11: 60,117,497-60,252,094 , GRCh38.p12 chr11: 60,350,024-60,484,621 MS4A1, MS4A7, 2 more genes
    nsv6131828inversion1nstd213human GRCh37 chr11: 60,117,497-60,252,092 , GRCh38.p12 chr11: 60,350,024-60,484,619 MS4A1, MS4A7, 2 more genes
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