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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5886386copy number variation1nstd209human GRCh38 chrY: 7,336,526-7,336,695 , GRCh37.p13 chrY: 7,204,567-7,204,736 PRKY
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5431206copy number variation1nstd206human GRCh38 chrY: 6,266,388-9,335,488 , GRCh37.p13 chrY: 6,134,429-9,173,097 , RN7SKP282, 76 more genes
    nsv5422484copy number variation1nstd206human GRCh38 chrY: 7,289,153-7,289,629 , GRCh37.p13 chrY: 7,157,194-7,157,670 PRKY
    nsv5332561translocation1nstd200human GRCh37 chrY: 7,166,583-7,166,583 , GRCh37 chrY: 7,166,651-7,166,651 , GRCh38.p12 chrY: 7,298,542-7,298,542 , GRCh38.p12 chrY: 7,298,610-7,298,610 PRKY
    nsv5200249mobile element insertion1nstd203human GRCh38 chrY: 7,331,742-7,331,750 , GRCh37.p13 chrY: 7,199,783-7,199,791 PRKY
    nsv5200248mobile element insertion1nstd203human GRCh38 chrY: 7,331,738-7,331,747 , GRCh37.p13 chrY: 7,199,779-7,199,788 PRKY
    nsv4909313copy number variation1nstd200human GRCh38 chrY: 6,811,997-7,746,934 , GRCh37.p13 chrY: 6,680,038-7,614,975 RN7SKP282, GPR143YP, 14 more genes
    nsv4902842copy number variation1nstd200human GRCh38 chrY: 7,272,075-7,517,063 , GRCh37.p13 chrY: 7,140,116-7,385,104 PRKY, RNU6-521P, 3 more genes
    nsv4730219inversion4nstd198human GRCh38 chrY: 6,198,014-9,936,872 , GRCh37.p13 chrY: 6,066,055-9,774,481 , AMELY, 109 more genes
    nsv4674256copy number variation1nstd102humanLikely benign GRCh37 chrY: 6,152,464-8,586,717 , GRCh38.p12 chrY: 6,284,423-8,718,676 LOC107987339, TTTY21B, 57 more genes
    nsv4674023copy number variation1nstd102humanUncertain significance GRCh37 chrY: 6,135,412-9,155,562 , GRCh38.p12 chrY: 6,267,371-9,317,953 MTND2P3, TBL1Y, 73 more genes
    nsv4674007copy number variation1nstd102humanLikely benign GRCh37 chrY: 6,172,777-9,168,128 , GRCh38.p12 chrY: 6,304,736-9,330,519 TSPY12P, GOT2P5, 74 more genes
    nsv4673949copy number variation1nstd102humanPathogenic GRCh37 chrY: 168,546-28,799,937 , GRCh38.p12 chrY: 301,879-26,653,790 GPM6BP2, TTTY18, 559 more genes
    nsv4673928copy number variation1nstd102humanPathogenic GRCh37 chrY: 1-16,095,773 , GRCh38.p12 chrY: 10,001-13,983,893 TTTY21, MTCO3P37, 239 more genes
    nsv4673881copy number variation1nstd102humanUncertain significance GRCh37 chrY: 6,371,105-7,342,674 , GRCh38.p12 chrY: 6,503,064-7,474,633 LOC107987338, ATP5PFP1, 11 more genes
    nsv4576040mobile element insertion1nstd166human GRCh37.p13 chrY: 7,199,779-7,199,779 , GRCh38.p12 chrY: 7,331,738-7,331,738 PRKY
    nsv4557663mobile element insertion1nstd166human GRCh37.p13 chrY: 7,213,192-7,213,192 , GRCh38.p12 chrY: 7,345,151-7,345,151 PRKY
    nsv4518361copy number variation1nstd166human GRCh37.p13 chrY: 6,359,999-8,576,000 , GRCh38.p12 chrY: 6,491,958-8,707,959 , FAM199YP, 49 more genes
    nsv4517160copy number variation1nstd166human GRCh37.p13 chrY: 7,097,999-7,331,200 , GRCh38.p12 chrY: 7,229,958-7,463,159 RN7SKP282, RNU6-941P, 3 more genes
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