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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6112709copy number variation1nstd102humanPathogenic GRCh37 chr3: 123,000,000-129,700,000 , GRCh38.p12 chr3: 123,281,153-129,981,157 OR7E97P, MARK3P3, 160 more genes
    nsv5608222insertion1nstd207human GRCh38 chr3: 129,394,598-129,394,598 , GRCh37.p13 chr3: 129,113,441-129,113,441 RPL32P3
    nsv5451171copy number variation1nstd206human GRCh38 chr3: 129,380,519-129,487,453 , GRCh37.p13 chr3: 129,099,362-129,206,296 IFT122, EFCAB12, 3 more genes
    nsv5448464copy number variation1nstd206human GRCh38 chr3: 129,389,249-129,389,436 , GRCh37.p13 chr3: 129,108,092-129,108,279 RPL32P3
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4914756copy number variation1nstd200human GRCh38 chr3: 129,384,416-129,491,454 , GRCh37.p13 chr3: 129,103,259-129,210,297 IFT122, EFCAB12, 3 more genes
    nsv4682966copy number variation1nstd102humanUncertain significance GRCh37 chr3: 128,889,296-129,270,183 , GRCh38.p12 chr3: 129,170,453-129,551,340 RPL32P3, NUP210P3, 17 more genes
    nsv4570212mobile element insertion1nstd166human GRCh37.p13 chr3: 129,108,516-129,108,516 , GRCh38.p12 chr3: 129,389,673-129,389,673 RPL32P3
    nsv4404482copy number variation1nstd174human GRCh37 chr3: 129,113,404-129,113,548 , GRCh38.p12 chr3: 129,394,561-129,394,705 RPL32P3
    nsv4403535copy number variation1nstd174human GRCh37 chr3: 129,099,664-129,213,583 , GRCh38.p12 chr3: 129,380,821-129,494,740 MBD4, SNORA7B, 3 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
    nsv4104854copy number variation1nstd166human GRCh37.p13 chr3: 129,111,000-129,217,000 , GRCh38.p12 chr3: 129,392,157-129,498,157 EFCAB12, IFT122, 3 more genes
    nsv4103683copy number variation1nstd166human GRCh37.p13 chr3: 129,108,115-129,108,259 , GRCh38.p12 chr3: 129,389,272-129,389,416 RPL32P3
    nsv3969257copy number variation1nstd168human GRCh38 chr3: 129,334,487-129,383,470 , GRCh37.p13 chr3: 129,053,330-129,102,313 RPL32P3, MARK2P3, 1 more genes
    nsv3967645insertion1nstd168human GRCh37.p13 chr3: 129,031,124-129,144,356 , GRCh38 chr3: 129,312,281-129,425,513 H1-10, EFCAB12, 6 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
    nsv3920834copy number variation1nstd102humanUncertain significance NCBI36 chr3: 127,308,312-142,119,621 , GRCh38 chr3: 126,106,779-140,918,089 , GRCh37 chr3: 125,825,622-140,636,931 NCK1-DT, LOC107986126, 271 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3912335copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 128,809,478-134,768,195 , GRCh37 chr3: 127,326,788-133,285,505 , GRCh38 chr3: 127,607,945-133,566,661 ACP3, FTH1P4, 130 more genes
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