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Items: 1 to 20 of 173

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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
    nsv7062877inversion1nstd229human GRCh38 chr11: 64,199,107-64,199,190 , GRCh37.p13 chr11: 63,966,579-63,966,662 STIP1
    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
    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
    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
    nsv6132371copy number variation1nstd213human GRCh37 chr11: 63,120,000-64,210,001 , GRCh38.p12 chr11: 63,352,528-64,442,529 VEGFB, FLRT1, 51 more genes
    nsv6132111copy number variation1nstd213human GRCh37 chr11: 63,900,000-64,180,001 , GRCh38.p12 chr11: 64,132,528-64,412,529 ESRRA, DNAJC4, 26 more genes
    nsv6039869copy number variation1nstd212human GRCh38 chr11: 64,199,627-64,199,793 , GRCh37.p13 chr11: 63,967,099-63,967,265 STIP1
    nsv6020903copy number variation1nstd212human GRCh38 chr11: 64,199,284-64,199,465 , GRCh37.p13 chr11: 63,966,756-63,966,937 STIP1
    nsv5920041copy number variation1nstd209human GRCh38 chr11: 64,186,267-64,193,073 , GRCh37.p13 chr11: 63,953,739-63,960,545 STIP1
    nsv5918368copy number variation1nstd209human GRCh38 chr11: 64,203,622-64,204,052 , GRCh37.p13 chr11: 63,971,094-63,971,524 STIP1
    nsv5916655copy number variation1nstd209human GRCh38 chr11: 64,194,620-64,195,643 , GRCh37.p13 chr11: 63,962,092-63,963,115 STIP1
    nsv5695485mobile element insertion1nstd211human GRCh38 chr11: 64,198,772-64,198,772 , GRCh37.p13 chr11: 63,966,244-63,966,244 STIP1
    nsv5494243copy number variation1nstd206human GRCh38 chr11: 64,180,429-64,184,401 , GRCh37.p13 chr11: 63,947,901-63,951,873 STIP1
    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
    nsv5344944translocation1nstd200human GRCh37 chr11: 63,961,657-63,961,657 , GRCh37 chr11: 63,960,760-63,960,760 , GRCh38.p12 chr11: 64,194,185-64,194,185 , GRCh38.p12 chr11: 64,193,288-64,193,288 STIP1
    nsv5274529copy number variation1nstd204human GRCh38.p13 chr11: 64,173,401-64,305,900 , GRCh37.p13 chr11: 63,940,873-64,073,372 LOC114841035, FKBP2, 15 more genes
    nsv5267852copy number variation1nstd204human GRCh38.p13 chr11: 64,173,401-65,676,300 , GRCh37.p13 chr11: 63,940,873-65,443,771 , TALAM1, 103 more genes
    nsv4979787copy number variation1nstd200human GRCh38 chr11: 64,198,338-64,199,669 , GRCh37.p13 chr11: 63,965,810-63,967,141 STIP1
    nsv4979786copy number variation1nstd200human GRCh38 chr11: 64,192,612-64,193,604 , GRCh37.p13 chr11: 63,960,084-63,961,076 STIP1
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