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Items: 1 to 20 of 871

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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
    nsv7073056inversion1nstd229human GRCh38 chr11: 122,322,692-122,333,654 , GRCh37.p13 chr11: 122,193,400-122,204,362 MIR100HG
    nsv7066711inversion1nstd229human GRCh38 chr11: 121,571,518-122,082,814 , GRCh37.p13 chr11: 121,442,227-121,953,522 SORL1, LOC107984402, 2 more genes
    nsv7066399inversion1nstd229human GRCh38 chr11: 122,315,195-122,328,122 , GRCh37.p13 chr11: 122,185,903-122,198,830 MIR100HG
    nsv7059023inversion1nstd229human GRCh38 chr11: 121,250,599-123,864,348 , GRCh37.p13 chr11: 121,121,308-123,735,056 MIR4493, SF3A3P2, 49 more genes
    nsv6917376copy number variation1nstd229human GRCh38 chr11: 122,341,201-122,349,700 , GRCh37.p13 chr11: 122,211,909-122,220,408 MIR100HG
    nsv6916384copy number variation1nstd229human GRCh38 chr11: 122,077,833-122,081,564 , GRCh37.p13 chr11: 121,948,541-121,952,272 MIR100HG
    nsv6915584copy number variation1nstd229human GRCh38 chr11: 122,406,773-122,410,792 , GRCh37.p13 chr11: 122,277,481-122,281,500 MIR100HG
    nsv6915135copy number variation1nstd229human GRCh38 chr11: 122,384,305-122,388,093 , GRCh37.p13 chr11: 122,255,013-122,258,801 MIR100HG
    nsv6912081copy number variation1nstd229human GRCh38 chr11: 122,326,590-122,326,962 , GRCh37.p13 chr11: 122,197,298-122,197,670 MIR100HG
    nsv6910850copy number variation1nstd229human GRCh38 chr11: 121,931,387-122,028,482 , GRCh37.p13 chr11: 121,802,095-121,899,190 MIR100HG, RNU6-256P
    nsv6910798copy number variation1nstd229human GRCh38 chr11: 122,061,076-122,067,444 , GRCh37.p13 chr11: 121,931,784-121,938,152 MIR100HG
    nsv6910556copy number variation1nstd229human GRCh38 chr11: 122,315,588-122,315,650 , GRCh37.p13 chr11: 122,186,296-122,186,358 MIR100HG
    nsv6910045copy number variation1nstd229human GRCh38 chr11: 122,229,136-122,235,255 , GRCh37.p13 chr11: 122,099,844-122,105,963 MIR100HG
    nsv6908824copy number variation1nstd229human GRCh38 chr11: 122,080,032-122,087,644 , GRCh37.p13 chr11: 121,950,740-121,958,352 MIR100HG
    nsv6908082copy number variation1nstd229human GRCh38 chr11: 122,191,001-122,195,800 , GRCh37.p13 chr11: 122,061,709-122,066,508 MIR100HG
    nsv6907009copy number variation1nstd229human GRCh38 chr11: 122,078,958-122,085,250 , GRCh37.p13 chr11: 121,949,666-121,955,958 MIR100HG
    nsv6907006copy number variation1nstd229human GRCh38 chr11: 122,070,301-122,072,900 , GRCh37.p13 chr11: 121,941,009-121,943,608 MIR100HG
    nsv6906904copy number variation1nstd229human GRCh38 chr11: 122,109,467-122,113,664 , GRCh37.p13 chr11: 121,980,175-121,984,372 MIR100HG, BLID
    nsv6905379copy number variation1nstd229human GRCh38 chr11: 122,296,785-122,299,483 , GRCh37.p13 chr11: 122,167,493-122,170,191 MIR100HG
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