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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7077001inversion1nstd229human GRCh38 chr11: 61,961,332-62,482,821 , GRCh37.p13 chr11: 61,728,804-62,250,293 SCGB2A1, INCENP, 16 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
    nsv6915655copy number variation1nstd229human GRCh38 chr11: 62,212,921-62,212,979 , GRCh37.p13 chr11: 61,980,393-61,980,451 SCGB2A1
    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
    nsv6903822copy number variation1nstd229human GRCh38 chr11: 62,209,635-62,237,836 , GRCh37.p13 chr11: 61,977,107-62,005,308 SCGB2A1
    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
    nsv6461104copy number variation1nstd223human GRCh38 chr11: 62,209,635-62,237,836 , GRCh37.p13 chr11: 61,977,107-62,005,308 SCGB2A1
    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
    nsv5973701insertion1nstd209human GRCh38 chr11: 62,212,961-62,212,961 , GRCh37.p13 chr11: 61,980,433-61,980,433 SCGB2A1
    nsv5917473copy number variation1nstd209human GRCh38 chr11: 62,209,635-62,237,812 , GRCh37.p13 chr11: 61,977,107-62,005,284 SCGB2A1
    nsv5855953copy number variation1nstd209human GRCh38 chr11: 62,209,444-62,236,971 , GRCh37.p13 chr11: 61,976,916-62,004,443 SCGB2A1
    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
    nsv4985009copy number variation1nstd200human GRCh38 chr11: 62,194,072-62,245,560 , GRCh37.p13 chr11: 61,961,544-62,013,032 SCGB2A1, SCGB1D2
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729555copy number variation1nstd102humanUncertain significance GRCh37 chr11: 61,874,941-62,236,378 , GRCh38.p12 chr11: 62,107,469-62,468,906 INCENP, SCGB2A1, 11 more genes
    nsv4675148copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,385,382-62,456,278 , GRCh38.p12 chr11: 60,617,909-62,688,806 LOC105369326, MS4A18, 91 more genes
    nsv4542819insertion1nstd166human GRCh37.p13 chr11: 61,979,058-61,979,058 , GRCh38.p12 chr11: 62,211,586-62,211,586 SCGB2A1
    nsv4527597copy number variation1nstd166human GRCh37.p13 chr11: 61,981,724-61,981,802 , GRCh38.p12 chr11: 62,214,252-62,214,330 SCGB2A1
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