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Items: 1 to 20 of 160

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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
    nsv5448642copy number variation1nstd206human GRCh38 chr3: 124,745,633-124,745,710 , GRCh37.p13 chr3: 124,464,480-124,464,557 UMPS
    nsv5346489translocation1nstd200human GRCh38 chr3: 124,366,225-124,366,225 , GRCh38 chr3: 124,749,336-124,749,336 , GRCh37.p13 chr3: 124,085,072-124,085,072 , GRCh37.p13 chr3: 124,468,183-124,468,183 UMPS, KALRN
    nsv5331180translocation1nstd200human GRCh37 chr3: 124,467,115-124,467,115 , GRCh37 chrX: 98,764,241-98,764,241 , GRCh38.p12 chr3: 124,748,268-124,748,268 , GRCh38.p12 chrX: 99,509,243-99,509,243 UMPS
    nsv5091957mobile element insertion1nstd203human GRCh38 chr3: 124,734,198-124,734,213 , GRCh37.p13 chr3: 124,453,045-124,453,060 UMPS, RPS26P22
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4587202copy number variation1nstd183human GRCh37 chr3: 124,441,695-124,503,671 , GRCh38.p12 chr3: 124,722,848-124,784,824 KALRN, MIR544B, 3 more genes
    nsv4521869copy number variation1nstd166human GRCh37.p13 chr3: 124,454,350-124,454,823 , GRCh38.p12 chr3: 124,735,503-124,735,976 UMPS
    nsv4521375copy number variation1nstd166human GRCh37.p13 chr3: 124,396,620-124,626,143 , GRCh38.p12 chr3: 124,677,773-124,907,296 ITGB5, UMPS, 5 more genes
    nsv4381835copy number variation1nstd173human GRCh37 chr3: 124,435,862-124,459,165 , GRCh38.p12 chr3: 124,717,015-124,740,318 RPS26P22, UMPS, 2 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
    nsv4091648copy number variation1nstd166human GRCh37.p13 chr3: 124,447,652-124,460,309 , GRCh38.p12 chr3: 124,728,805-124,741,462 MIR544B, RPS26P22, 1 more genes
    nsv3924082copy number variation1nstd102humanPathogenic NCBI36 chr3: 119,875,435-127,742,263 , GRCh38 chr3: 118,673,898-126,540,730 , GRCh37 chr3: 118,392,745-126,259,573 MYLK-AS2, RPL7AP11, 165 more genes
    nsv3923097copy number variation1nstd102humanPathogenic NCBI36 chr3: 120,318,703-127,122,267 , GRCh38 chr3: 119,117,166-125,920,734 , GRCh37 chr3: 118,836,013-125,639,577 POGLUT1, RN7SL397P, 141 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
    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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