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Items: 1 to 20 of 114

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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
    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
    nsv6474584copy number variation1nstd223human GRCh38 chr11: 64,318,001-64,319,700 , GRCh37.p13 chr11: 64,085,473-64,087,172 PRDX5, TRMT112
    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
    nsv5497068copy number variation1nstd206human GRCh38 chr11: 64,317,986-64,320,108 , GRCh37.p13 chr11: 64,085,458-64,087,580 TRMT112, PRDX5
    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
    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
    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
    nsv4673562copy number variation1nstd186human GRCh37 chr11: 64,085,461-64,087,581 , GRCh38.p12 chr11: 64,317,989-64,320,109 PRDX5, TRMT112
    nsv4608241copy number variation2nstd183human GRCh37 chr11: 64,085,418-64,087,410 , GRCh38.p12 chr11: 64,317,946-64,319,938 PRDX5, TRMT112
    nsv4600337copy number variation1nstd183human GRCh37 chr11: 64,085,461-64,087,581 , GRCh38.p12 chr11: 64,317,989-64,320,109 PRDX5, TRMT112
    nsv4436237copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 63,533,279-65,429,676 , GRCh38.p12 chr11: 63,765,807-65,662,205 ARL2, BAD, 117 more genes
    nsv4198741copy number variation1nstd166human GRCh37.p13 chr11: 64,085,458-64,087,580 , GRCh38.p12 chr11: 64,317,986-64,320,108 TRMT112, PRDX5
    nsv3959904copy number variation1nstd168human GRCh38 chr11: 64,314,606-64,343,227 , GRCh37.p13 chr11: 64,082,078-64,110,699 ESRRA, PRDX5, 4 more genes
    nsv3924003copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 62,417,274-63,859,091 , GRCh37 chr11: 62,660,698-64,102,515 , GRCh38 chr11: 62,893,226-64,335,043 BAD, CCND2P1, 58 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
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