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Items: 1 to 20 of 142

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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
    nsv6910366copy number variation1nstd229human GRCh38 chr11: 64,225,715-64,226,338 , GRCh37.p13 chr11: 63,993,187-63,993,810 TRPT1, NUDT22
    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
    nsv6902745copy number variation1nstd229human GRCh38 chr11: 64,221,452-64,224,072 , GRCh37.p13 chr11: 63,988,924-63,991,544 TRPT1, FERMT3
    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
    nsv6309118copy number variation1nstd102humanUncertain significance GRCh37 chr11: 63,974,837-63,990,964 , GRCh38.p12 chr11: 64,207,365-64,223,492 FERMT3, TRPT1
    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
    nsv5923703copy number variation1nstd209human GRCh38 chr11: 64,221,692-64,222,001 , GRCh37.p13 chr11: 63,989,164-63,989,473 FERMT3, TRPT1
    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
    nsv5318731copy number variation1nstd204human GRCh38.p13 chr11: 64,216,488-64,260,689 , GRCh37.p13 chr11: 63,983,960-64,028,161 FKBP2, PPP1R14B-AS1, 8 more genes
    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
    nsv5273509copy number variation1nstd204human GRCh38.p13 chr11: 64,216,492-64,229,460 , GRCh37.p13 chr11: 63,983,964-63,996,932 TRPT1, DNAJC4, 2 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
    nsv5263110copy number variation1nstd204human GRCh37.p13 chr11: 63,981,273-64,014,072 , GRCh38.p13 chr11: 64,213,801-64,246,600 FKBP2, DNAJC4, 7 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
    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
    nsv4193765copy number variation1nstd166human GRCh37.p13 chr11: 63,993,260-63,993,876 , GRCh38.p12 chr11: 64,225,788-64,226,404 NUDT22, TRPT1
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