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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3924118copy number variation1nstd102humanPathogenic GRCh38 chr7: 120,795,527-120,842,557 , NCBI36 chr7: 120,222,817-120,269,847 , GRCh37 chr7: 120,435,581-120,482,611 TSPAN12
    nsv7097343copy number variation1nstd102humanPathogenic GRCh37 chr7: 120,428,646-120,446,766 , GRCh38.p12 chr7: 120,788,592-120,806,712 TSPAN12
    nsv5673843copy number variation1nstd102humanPathogenic GRCh37 chr7: 120,428,646-120,446,746 , GRCh38.p12 chr7: 120,788,592-120,806,692 TSPAN12
    nsv7097477copy number variation1nstd102humanPathogenic GRCh37 chr7: 120,478,811-120,478,986 , GRCh38.p12 chr7: 120,838,757-120,838,932 TSPAN12
    nsv4683601copy number variation1nstd102humanPathogenic GRCh37 chr7: 120,496,752-120,496,817 , GRCh38.p12 chr7: 120,856,698-120,856,763 TSPAN12
    nsv6312429copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 120,478,811-120,480,183 , GRCh38.p12 chr7: 120,838,757-120,840,129 TSPAN12
    nsv3903971copy number variation1nstd102humanBenign GRCh37 chr7: 119,388,127-119,577,292 , GRCh38.p12 chr7: 119,748,073-119,937,238 LINC02476
    nsv3894793copy number variation1nstd102humanBenign GRCh37 chr7: 119,366,996-119,401,720 , GRCh38.p12 chr7: 119,726,942-119,761,666 LINC02476
    nsv3891478copy number variation1nstd102humanBenign GRCh37 chr7: 119,366,996-119,388,127 , GRCh38.p12 chr7: 119,726,942-119,748,073 LINC02476
    nsv3893348copy number variation1nstd102humanBenign GRCh37 chr7: 119,375,538-119,384,595 , GRCh38.p12 chr7: 119,735,484-119,744,541 LINC02476
    nsv6312522copy number variation1nstd102humanUncertain significance GRCh37 chr7: 120,428,646-120,496,817 , GRCh38.p12 chr7: 120,788,592-120,856,763 TSPAN12
    nsv6312428copy number variation1nstd102humanUncertain significance GRCh37 chr7: 120,428,646-120,428,971 , GRCh38.p12 chr7: 120,788,592-120,788,917 TSPAN12
    nsv4683078copy number variation1nstd102humanUncertain significance GRCh37 chr7: 120,428,646-120,428,951 , GRCh38.p12 chr7: 120,788,592-120,788,897 TSPAN12
    nsv3912584copy number variation1nstd102humanUncertain significance NCBI36 chr7: 119,078,781-119,405,026 , GRCh37.p13 chr7: 119,291,545-119,617,790 , GRCh38.p12 chr7: 119,651,491-119,977,736 LINC02476, LOC107986840
    nsv6313635copy number variation1nstd102humanUncertain significance GRCh37 chr7: 120,330,665-120,481,519 , GRCh38.p12 chr7: 120,690,611-120,841,465 TSPAN12, KCND2
    nsv4683123copy number variation1nstd102humanUncertain significance GRCh37 chr7: 120,372,957-120,480,163 , GRCh38.p12 chr7: 120,732,903-120,840,109 TSPAN12, KCND2
    nsv7097476copy number variation1nstd102humanUncertain significance GRCh37 chr7: 120,387,715-120,428,971 , GRCh38.p12 chr7: 120,747,661-120,788,917 TSPAN12, KCND2
    nsv6312521copy number variation1nstd102humanUncertain significance GRCh37 chr7: 119,914,687-120,496,817 , GRCh38.p12 chr7: 120,274,633-120,856,763 TSPAN12, KCND2, 1 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 TSPAN12, RNU6-438P, 2682 more genes
    nsv3888815copy number variation1nstd102humanPathogenic GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467 TSPAN12, LOC107986817, 2014 more genes
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