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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
    nsv7052094inversion1nstd229human GRCh38 chr3: 132,609,279-139,052,095 , GRCh37.p13 chr3: 132,328,123-138,770,937 RNU6-789P, UBA5, 98 more genes
    nsv7044513inversion1nstd229human GRCh38 chr3: 131,210,998-138,882,695 , GRCh37.p13 chr3: 130,929,842-138,601,537 HSPA8P9, RNU6-1174P, 114 more genes
    nsv7039302inversion1nstd229human GRCh38 chr3: 133,378,933-139,551,784 , GRCh37.p13 chr3: 133,097,777-139,270,626 ESYT3, DONSONP1, 99 more genes
    nsv7039034inversion1nstd229human GRCh38 chr3: 136,134,661-138,768,814 , GRCh37.p13 chr3: 135,853,503-138,487,656 KRT8P36, RPL31P23, 37 more genes
    nsv6723684copy number variation1nstd229human GRCh38 chr3: 136,844,558-136,846,890 , GRCh37.p13 chr3: 136,563,400-136,565,732 NCK1-DT, SLC35G2
    nsv6722937copy number variation1nstd229human GRCh38 chr3: 136,813,721-138,134,157 , GRCh37.p13 chr3: 136,532,563-137,852,999 LOC105374128, IL20RB-AS1, 17 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6556098inversion1nstd223human GRCh38 chr3: 136,849,410-136,849,999 , GRCh37.p13 chr3: 136,568,252-136,568,841 SLC35G2, NCK1-DT
    nsv6357834copy number variation1nstd223human GRCh38 chr3: 136,843,219-136,844,114 , GRCh37.p13 chr3: 136,562,061-136,562,956 NCK1-DT, SLC35G2
    nsv6357282copy number variation1nstd223human GRCh38 chr3: 136,849,745-136,852,745 , GRCh37.p13 chr3: 136,568,587-136,571,587 NCK1-DT, SLC35G2
    nsv6291145copy number variation1nstd102humanUncertain significance GRCh37 chr3: 136,358,576-136,577,368 , GRCh38.p12 chr3: 136,639,734-136,858,526 DNAJC8P2, STAG1, 3 more genes
    nsv6134786copy number variation1nstd213human GRCh37 chr3: 136,540,000-136,610,001 , GRCh38.p12 chr3: 136,821,158-136,891,159 NCK1, SLC35G2, 1 more genes
    nsv6134785copy number variation1nstd213human GRCh37 chr3: 135,840,000-139,360,001 , GRCh38.p12 chr3: 136,121,158-139,641,159 ACTG1P1, FOXL2, 59 more genes
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    nsv5902204copy number variation1nstd209human GRCh38 chr3: 136,844,541-136,846,902 , GRCh37.p13 chr3: 136,563,383-136,565,744 NCK1-DT, SLC35G2
    nsv5834674copy number variation1nstd209human GRCh38 chr3: 136,844,861-136,846,777 , GRCh37.p13 chr3: 136,563,703-136,565,619 SLC35G2, NCK1-DT
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4927963copy number variation1nstd200human GRCh38 chr3: 136,860,216-136,861,613 , GRCh37.p13 chr3: 136,579,058-136,580,455 NCK1, NCK1-DT
    nsv4927962copy number variation1nstd200human GRCh38 chr3: 136,847,509-136,847,789 , GRCh37.p13 chr3: 136,566,351-136,566,631 NCK1-DT, SLC35G2
    nsv4927961copy number variation1nstd200human GRCh38 chr3: 136,844,556-136,846,889 , GRCh37.p13 chr3: 136,563,398-136,565,731 SLC35G2, NCK1-DT
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