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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097477copy number variation1nstd102humanPathogenic GRCh37 chr7: 120,478,811-120,478,986 , GRCh38.p12 chr7: 120,838,757-120,838,932 TSPAN12
    nsv7097476copy number variation1nstd102humanUncertain significance GRCh37 chr7: 120,387,715-120,428,971 , GRCh38.p12 chr7: 120,747,661-120,788,917 KCND2, TSPAN12
    nsv7097343copy number variation1nstd102humanPathogenic GRCh37 chr7: 120,428,646-120,446,766 , GRCh38.p12 chr7: 120,788,592-120,806,712 TSPAN12
    nsv7056817inversion1nstd229human GRCh38 chr7: 120,820,049-120,929,181 , GRCh37.p13 chr7: 120,460,103-120,569,235 TSPAN12
    nsv7055882inversion1nstd229human GRCh38 chr7: 120,635,987-120,825,724 , GRCh37.p13 chr7: 120,276,041-120,465,778 KCND2, TSPAN12, 1 more genes
    nsv7052394inversion1nstd229human GRCh38 chr7: 120,630,873-120,821,682 , GRCh37.p13 chr7: 120,270,927-120,461,736 KCND2, TSPAN12, 1 more genes
    nsv7043376inversion1nstd229human GRCh38 chr7: 120,819,126-120,831,304 , GRCh37.p13 chr7: 120,459,180-120,471,358 TSPAN12
    nsv6835587copy number variation1nstd229human GRCh38 chr7: 120,754,501-120,807,400 , GRCh37.p13 chr7: 120,394,555-120,447,454 TSPAN12
    nsv6834057copy number variation1nstd229human GRCh38 chr7: 120,779,301-120,786,600 , GRCh37.p13 chr7: 120,419,355-120,426,654 TSPAN12
    nsv6829122copy number variation1nstd229human GRCh38 chr7: 120,836,426-120,836,761 , GRCh37.p13 chr7: 120,476,480-120,476,815 TSPAN12
    nsv6826575copy number variation1nstd229human GRCh38 chr7: 120,846,539-120,846,710 , GRCh37.p13 chr7: 120,486,593-120,486,764 TSPAN12
    nsv6826108copy number variation1nstd229human GRCh38 chr7: 120,794,707-120,795,045 , GRCh37.p13 chr7: 120,434,761-120,435,099 TSPAN12
    nsv6825744copy number variation1nstd229human GRCh38 chr7: 120,119,180-121,466,883 , GRCh37.p13 chr7: 119,759,234-121,106,937 WNT16, CYCSP19, 12 more genes
    nsv6823153copy number variation1nstd229human GRCh38 chr7: 120,788,443-120,790,640 , GRCh37.p13 chr7: 120,428,497-120,430,694 TSPAN12
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6612047copy number variation1nstd223human GRCh38 chr7: 120,830,301-120,832,000 , GRCh37.p13 chr7: 120,470,355-120,472,054 TSPAN12
    nsv6609017copy number variation1nstd223human GRCh38 chr7: 120,802,601-120,804,400 , GRCh37.p13 chr7: 120,442,655-120,444,454 TSPAN12
    nsv6608754copy number variation1nstd223human GRCh38 chr7: 120,818,401-120,819,000 , GRCh37.p13 chr7: 120,458,455-120,459,054 TSPAN12
    nsv6608072copy number variation1nstd223human GRCh38 chr7: 120,839,903-120,840,249 , GRCh37.p13 chr7: 120,479,957-120,480,303 TSPAN12
    nsv6607778copy number variation1nstd223human GRCh38 chr7: 120,802,702-120,803,322 , GRCh37.p13 chr7: 120,442,756-120,443,376 TSPAN12
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