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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074145inversion1nstd229human GRCh38 chr11: 104,112,094-113,544,164 , GRCh37.p13 chr11: 103,982,822-113,414,886 COLCA1, LOC105369491, 150 more genes
    nsv7068895inversion1nstd229human GRCh38 chr11: 100,518,680-109,308,656 , GRCh37.p13 chr11: 100,389,411-109,179,383 LINC02719, RNA5SP349, 121 more genes
    nsv7067245inversion1nstd229human GRCh38 chr11: 103,215,092-107,313,893 , GRCh37.p13 chr11: 103,085,821-107,184,619 DYNC2H1, LINC02719, 51 more genes
    nsv7063726inversion1nstd229human GRCh38 chr11: 105,350,510-106,541,812 , GRCh37.p13 chr11: 105,221,237-106,412,539 RNU4-55P, RNU6-277P, 10 more genes
    nsv6917097copy number variation1nstd229human GRCh38 chr11: 106,117,968-106,125,167 , GRCh37.p13 chr11: 105,988,695-105,995,894 LINC02719
    nsv6913653copy number variation1nstd229human GRCh38 chr11: 106,116,472-106,118,197 , GRCh37.p13 chr11: 105,987,199-105,988,924 LINC02719
    nsv6907676copy number variation1nstd229human GRCh38 chr11: 104,112,085-107,043,966 , GRCh37.p13 chr11: 103,982,813-106,914,692 GUCY1A2, LINC02719, 36 more genes
    nsv6904732copy number variation1nstd229human GRCh38 chr11: 106,050,526-106,182,561 , GRCh37.p13 chr11: 105,921,253-106,053,288 LINC02719, AASDHPPT, 1 more genes
    nsv6901490copy number variation1nstd229human GRCh38 chr11: 106,106,909-106,112,998 , GRCh37.p13 chr11: 105,977,636-105,983,725 LINC02719
    nsv6899201copy number variation1nstd229human GRCh38 chr11: 106,131,243-106,135,943 , GRCh37.p13 chr11: 106,001,970-106,006,670 LINC02719
    nsv6637687copy number variation1nstd102humanPathogenic GRCh37 chr11: 101,371,503-109,306,519 , GRCh38.p12 chr11: 101,500,772-109,435,793 GRIA4, MTND1P36, 111 more genes
    nsv6583546inversion1nstd223human GRCh38 chr11: 105,350,509-106,541,811 , GRCh37.p13 chr11: 105,221,236-106,412,538 LINC02719, RNU4-55P, 10 more genes
    nsv6578547inversion1nstd223human GRCh38 chr11: 104,070,004-110,020,477 , GRCh37.p13 chr11: 103,940,732-109,891,203 ACAT1, RNU6-654P, 69 more genes
    nsv6475350copy number variation1nstd223human GRCh38 chr11: 104,112,101-107,043,900 , GRCh37.p13 chr11: 103,982,829-106,914,626 LOC107984381, LOC100422300, 36 more genes
    nsv6468321copy number variation1nstd223human GRCh38 chr11: 105,876,428-106,324,128 , GRCh37.p13 chr11: 105,747,154-106,194,855 GRIA4, AASDHPPT, 6 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
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv6131907copy number variation1nstd213human GRCh37 chr11: 104,930,000-106,230,001 , GRCh38.p12 chr11: 105,059,273-106,359,274 OR2AL1P, CASP1P3, 17 more genes
    nsv5918104copy number variation1nstd209human GRCh38 chr11: 104,190,618-110,044,159 , GRCh37.p13 chr11: 104,061,346-109,914,884 , CARD18, 71 more genes
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