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Items: 1 to 20 of 105

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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
    nsv5951882insertion1nstd209human GRCh38 chr3: 129,530,533-129,530,533 , GRCh37.p13 chr3: 129,249,376-129,249,376 RHO
    nsv5693602mobile element insertion1nstd211human GRCh38 chr3: 129,535,156-129,535,156 , GRCh37.p13 chr3: 129,253,999-129,253,999 RHO
    nsv5438284copy number variation1nstd206human GRCh38 chr3: 129,533,027-129,533,196 , GRCh37.p13 chr3: 129,251,870-129,252,039 RHO
    nsv5381590copy number variation1nstd102humanUncertain significance GRCh37 chr3: 129,234,311-129,252,561 , GRCh38.p12 chr3: 129,515,468-129,533,718 RHO, IFT122
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4914757copy number variation1nstd200human GRCh38 chr3: 129,531,560-129,546,880 , GRCh37.p13 chr3: 129,250,403-129,265,723 RHO, H1-8
    nsv4804812copy number variation1nstd200human GRCh37 chr3: 129,250,403-129,265,723 , GRCh38.p12 chr3: 129,531,560-129,546,880 H1-8, RHO
    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
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4104079copy number variation1nstd166human GRCh37.p13 chr3: 129,251,870-129,252,039 , GRCh38.p12 chr3: 129,533,027-129,533,196 RHO
    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
    nsv3889515copy number variation1nstd102humanBenign GRCh37 chr3: 129,239,972-129,350,751 , GRCh38.p12 chr3: 129,521,129-129,631,908 RN7SL752P, H1-8, 2 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3883666copy number variation1nstd102humanUncertain significance GRCh37 chr3: 128,660,985-129,811,200 , GRCh38.p12 chr3: 128,942,142-130,092,357 RHO, GP9, 35 more genes
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