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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv5344774translocation1nstd200human GRCh37 chr3: 126,390,884-126,390,884 , GRCh37 chr3: 126,391,041-126,391,041 , GRCh38.p12 chr3: 126,672,041-126,672,041 , GRCh38.p12 chr3: 126,672,198-126,672,198 NUP210P1, SF3A2P1
    nsv5305991copy number variation1nstd204human GRCh37.p13 chr3: 126,390,878-126,391,049 , GRCh38.p13 chr3: 126,672,035-126,672,206 NUP210P1, SF3A2P1
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4587216copy number variation1nstd183human GRCh37 chr3: 126,326,116-126,388,335 , GRCh38.p12 chr3: 126,607,273-126,669,492 NUP210P1, TXNRD3, 1 more genes
    nsv4387884copy number variation1nstd173human GRCh37 chr3: 126,326,103-126,388,334 , GRCh38.p12 chr3: 126,607,260-126,669,491 NUP210P1, METTL5P2, 1 more genes
    nsv4368647copy number variation1nstd173human GRCh37 chr3: 125,803,412-126,619,202 , GRCh38.p12 chr3: 126,084,569-126,900,359 CFAP100-DT, RCC2P4, 24 more genes
    nsv4347357copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 124,369,671-126,423,192 , GRCh38.p12 chr3: 124,650,824-126,704,349 ITGB5, UMPS, 63 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
    nsv4082024copy number variation1nstd166human GRCh37.p13 chr3: 126,160,795-126,686,832 , GRCh38.p12 chr3: 126,441,952-126,967,989 ZXDC, METTL5P2, 10 more genes
    nsv4079067copy number variation1nstd166human GRCh37.p13 chr3: 126,388,331-126,391,382 , GRCh38.p12 chr3: 126,669,488-126,672,539 SF3A2P1, NUP210P1
    nsv4076110copy number variation1nstd166human GRCh37.p13 chr3: 126,352,548-126,383,856 , GRCh38.p12 chr3: 126,633,705-126,665,013 NUP210P1, TXNRD3
    nsv3963902insertion1nstd168human GRCh38 chr3: 126,642,962-126,664,649 , GRCh37.p13 chr3: 126,361,805-126,383,492 NUP210P1, TXNRD3
    nsv3956206copy number variation1nstd168human GRCh38 chr3: 126,663,758-126,682,180 , GRCh37.p13 chr3: 126,382,601-126,401,023 NUP210P1, SF3A2P1
    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
    nsv3918094copy number variation1nstd102humanPathogenic NCBI36 chr3: 113,822,514-129,935,667 , GRCh38 chr3: 112,620,977-128,734,134 , GRCh37 chr3: 112,339,824-128,452,977 QTRT2, MIR544B, 284 more genes
    nsv3913250copy number variation1nstd102humanPathogenic NCBI36 chr3: 123,126,684-127,983,782 , GRCh38 chr3: 121,925,147-126,782,249 , GRCh37 chr3: 121,643,994-126,501,092 RPS24P9, ADCY5, 106 more genes
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