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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7044478inversion1nstd229human GRCh38 chr3: 140,992,844-142,136,153 , GRCh37.p13 chr3: 140,711,686-141,854,995 KRT18P35, SPSB4, 16 more genes
    nsv6736931copy number variation1nstd229human GRCh38 chr3: 141,137,997-141,260,842 , GRCh37.p13 chr3: 140,856,839-140,979,684 RPL31P21, SPSB4, 1 more genes
    nsv6731718copy number variation1nstd229human GRCh38 chr3: 140,970,345-141,440,016 , GRCh37.p13 chr3: 140,689,187-141,158,858 SPSB4, PHF5AP7, 4 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
    nsv6134994copy number variation1nstd213human GRCh37 chr3: 139,490,000-150,360,001 , GRCh38.p12 chr3: 139,771,158-150,642,214 , ATP1B3, 147 more genes
    nsv6134670copy number variation1nstd213human GRCh37 chr3: 140,890,000-141,020,001 , GRCh38.p12 chr3: 141,171,158-141,301,159 PXYLP1, RPL31P21
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034922inversion1nstd200human GRCh38 chr3: 137,979,992-148,451,901 , GRCh37.p13 chr3: 137,698,834-148,169,688 , LOC105374148, 132 more genes
    nsv4914822copy number variation1nstd200human GRCh38 chr3: 141,109,396-141,330,220 , GRCh37.p13 chr3: 140,828,238-141,049,062 RPL31P21, PHF5AP7, 3 more genes
    nsv4873274inversion1nstd200human GRCh37 chr3: 137,698,834-148,169,688 , GRCh38.p12 chr3: 137,979,992-148,451,901 , PLSCR5, 132 more genes
    nsv4728275copy number variation1nstd102humanUncertain significance GRCh37 chr3: 140,829,421-141,154,102 , GRCh38.p12 chr3: 141,110,579-141,435,260 PXYLP1, SPSB4, 3 more genes
    nsv4728141copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,737,687-142,053,396 , GRCh38.p12 chr3: 139,018,845-142,334,554 RNU6-425P, YWHAQP6, 41 more genes
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
    nsv4347615copy number variation1nstd102humanPathogenic GRCh37 chr3: 135,288,025-146,874,012 , GRCh38.p12 chr3: 135,569,183-147,156,225 RPL6P9, NME9, 145 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4327115inversion1nstd166human GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530 , ATP1B3, 446 more genes
    nsv3923685copy number variation1nstd102humanPathogenic GRCh37 chr3: 137,650,842-144,187,581 , NCBI36 chr3: 139,133,532-145,670,271 , GRCh38 chr3: 137,932,000-144,468,739 ATP1B3, RPL23AP40, 97 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3921636copy number variation1nstd102humanPathogenic GRCh38 chr3: 135,227,451-145,870,770 , NCBI36 chr3: 136,428,983-147,071,247 , GRCh37 chr3: 134,946,293-145,588,557 A4GNT, TRIM42, 134 more genes
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