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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5600432copy number variation1nstd207human GRCh38 chr15: 43,747,391-43,747,745 , GRCh37.p13 chr15: 44,039,589-44,039,943 PDIA3
    nsv5597957copy number variation1nstd207human GRCh38 chr15: 43,745,472-43,745,779 , GRCh37.p13 chr15: 44,037,670-44,037,977 CATSPER2P1, PDIA3
    nsv5512663copy number variation1nstd206human GRCh38 chr15: 43,718,874-43,744,874 , GRCh37.p13 chr15: 44,011,072-44,037,072 RNU6-354P, PDIA3, 1 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5380053translocation1nstd200human GRCh38 chr15: 43,755,295-43,755,295 , GRCh38 chr15: 43,626,868-43,626,868 , GRCh37.p13 chr15: 43,919,066-43,919,066 , GRCh37.p13 chr15: 44,047,493-44,047,493 CATSPER2, PDIA3
    nsv5335555translocation1nstd200human GRCh37 chr15: 43,919,066-43,919,066 , GRCh37 chr15: 44,047,493-44,047,493 , GRCh38.p12 chr15: 43,626,868-43,626,868 , GRCh38.p12 chr15: 43,755,295-43,755,295 PDIA3, CATSPER2
    nsv5302493copy number variation1nstd204human GRCh38.p13 chr15: 43,748,312-43,749,599 , GRCh37.p13 chr15: 44,040,510-44,041,797 PDIA3
    nsv5187204mobile element insertion1nstd203human GRCh38 chr15: 43,759,383-43,759,383 , GRCh37.p13 chr15: 44,051,581-44,051,581 PDIA3
    nsv5146539mobile element insertion1nstd203human GRCh38 chr15: 43,745,593-43,745,600 , GRCh37.p13 chr15: 44,037,791-44,037,798 PDIA3, CATSPER2P1
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5005328copy number variation1nstd200human GRCh38 chr15: 43,648,494-43,746,065 , GRCh37.p13 chr15: 43,940,692-44,038,263 PPIP5K1P1-CATSPER2, PDIA3P2, 8 more genes
    nsv5001514copy number variation1nstd200human GRCh38 chr15: 43,772,321-43,772,511 , GRCh37.p13 chr15: 44,064,519-44,064,709 ELL3, PDIA3
    nsv5001513copy number variation1nstd200human GRCh38 chr15: 43,757,387-43,760,970 , GRCh37.p13 chr15: 44,049,585-44,053,168 PDIA3
    nsv5001512copy number variation1nstd200human GRCh38 chr15: 43,748,304-43,749,535 , GRCh37.p13 chr15: 44,040,502-44,041,733 PDIA3
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4865955copy number variation1nstd200human GRCh37 chr15: 44,037,138-44,038,099 , GRCh38.p12 chr15: 43,744,940-43,745,901 PDIA3, CATSPER2P1
    nsv4675221copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,420,601-44,198,616 , GRCh38.p12 chr15: 43,128,403-43,906,418 TGM5, CATSPER2P1, 38 more genes
    nsv4502181mobile element insertion1nstd166human GRCh37.p13 chr15: 44,049,066-44,049,066 , GRCh38.p12 chr15: 43,756,868-43,756,868 PDIA3
    nsv4424147copy number variation1nstd174human GRCh37 chr15: 43,831,879-44,054,734 , GRCh38.p12 chr15: 43,539,681-43,762,536 CATSPER2, STRC, 13 more genes
    nsv4415186copy number variation1nstd174human GRCh37 chr15: 43,914,749-44,040,886 , GRCh38.p12 chr15: 43,622,551-43,748,688 PDIA3, RNU6-354P, 9 more genes
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