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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5848601copy number variation1nstd209human GRCh38 chr15: 43,727,291-43,743,597 , GRCh37.p13 chr15: 44,019,489-44,035,795 RNU6-354P, CATSPER2P1
    nsv5644823insertion1nstd207human GRCh38 chr15: 43,739,806-43,739,806 , GRCh37.p13 chr15: 44,032,004-44,032,004 CATSPER2P1
    nsv5602723copy number variation1nstd207human GRCh38 chr15: 43,740,633-43,740,881 , GRCh37.p13 chr15: 44,032,831-44,033,079 CATSPER2P1
    nsv5599032copy number variation1nstd207human GRCh38 chr15: 43,742,861-43,743,133 , GRCh37.p13 chr15: 44,035,059-44,035,331 CATSPER2P1
    nsv5597957copy number variation1nstd207human GRCh38 chr15: 43,745,472-43,745,779 , GRCh37.p13 chr15: 44,037,670-44,037,977 CATSPER2P1, PDIA3
    nsv5596311copy number variation1nstd207human GRCh38 chr15: 43,739,797-43,740,112 , GRCh37.p13 chr15: 44,031,995-44,032,310 CATSPER2P1
    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
    nsv5511934copy number variation1nstd206human GRCh38 chr15: 43,742,477-43,743,031 , GRCh37.p13 chr15: 44,034,675-44,035,229 CATSPER2P1
    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
    nsv5380052translocation1nstd200human GRCh38 chr15: 43,624,401-43,624,401 , GRCh38 chr15: 43,740,766-43,740,766 , GRCh37.p13 chr15: 43,916,599-43,916,599 , GRCh37.p13 chr15: 44,032,964-44,032,964 CATSPER2P1
    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
    nsv5001511copy number variation1nstd200human GRCh38 chr15: 43,734,678-43,736,032 , GRCh37.p13 chr15: 44,026,876-44,028,230 RNU6-354P, CATSPER2P1
    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
    nsv4865954copy number variation1nstd200human GRCh37 chr15: 44,026,833-44,028,240 , GRCh38.p12 chr15: 43,734,635-43,736,042 CATSPER2P1, RNU6-354P
    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
    nsv4425344copy number variation1nstd174human GRCh37 chr15: 43,924,475-44,033,981 , GRCh38.p12 chr15: 43,632,277-43,741,783 PDIA3P2, RNU6-610P, 8 more genes
    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
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