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Items: 1 to 20 of 413

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7067797inversion1nstd229human GRCh38 chr15: 48,940,548-48,959,927 , GRCh37.p13 chr15: 49,232,745-49,252,124 SHC4
    nsv7067502inversion1nstd229human GRCh38 chr15: 48,513,881-51,354,383 , GRCh37.p13 chr15: 48,806,078-51,646,580 NDUFAF4P1, MIR4713, 49 more genes
    nsv6976281copy number variation1nstd229human GRCh38 chr15: 48,886,247-48,888,876 , GRCh37.p13 chr15: 49,178,444-49,181,073 SHC4
    nsv6975049copy number variation1nstd229human GRCh38 chr15: 48,959,501-48,966,000 , GRCh37.p13 chr15: 49,251,698-49,258,197 SHC4
    nsv6973985copy number variation1nstd229human GRCh38 chr15: 48,814,737-48,848,490 , GRCh37.p13 chr15: 49,106,934-49,140,687 SHC4
    nsv6973571copy number variation1nstd229human GRCh38 chr15: 48,962,592-48,973,257 , GRCh37.p13 chr15: 49,254,789-49,265,454 SHC4, KRT8P24
    nsv6970449copy number variation1nstd229human GRCh38 chr15: 48,849,555-48,856,607 , GRCh37.p13 chr15: 49,141,752-49,148,804 SHC4
    nsv6969086copy number variation1nstd229human GRCh38 chr15: 48,946,617-48,964,508 , GRCh37.p13 chr15: 49,238,814-49,256,705 SHC4
    nsv6968771copy number variation1nstd229human GRCh38 chr15: 48,771,078-48,838,415 , GRCh37.p13 chr15: 49,063,275-49,130,612 CEP152, SHC4
    nsv6968760copy number variation1nstd229human GRCh38 chr15: 48,907,101-48,914,100 , GRCh37.p13 chr15: 49,199,298-49,206,297 SHC4
    nsv6967196copy number variation1nstd229human GRCh38 chr15: 48,960,954-48,975,519 , GRCh37.p13 chr15: 49,253,151-49,267,716 SHC4, KRT8P24
    nsv6966076copy number variation1nstd229human GRCh38 chr15: 48,888,468-48,888,803 , GRCh37.p13 chr15: 49,180,665-49,181,000 SHC4
    nsv6965991copy number variation1nstd229human GRCh38 chr15: 48,905,066-48,908,751 , GRCh37.p13 chr15: 49,197,263-49,200,948 SHC4
    nsv6964636copy number variation1nstd229human GRCh38 chr15: 48,821,319-48,823,629 , GRCh37.p13 chr15: 49,113,516-49,115,826 SHC4
    nsv6962408copy number variation1nstd229human GRCh38 chr15: 48,927,581-48,951,030 , GRCh37.p13 chr15: 49,219,778-49,243,227 SHC4
    nsv6960839copy number variation1nstd229human GRCh38 chr15: 48,911,662-48,919,677 , GRCh37.p13 chr15: 49,203,859-49,211,874 SHC4
    nsv6960252copy number variation1nstd229human GRCh38 chr15: 48,896,702-48,904,011 , GRCh37.p13 chr15: 49,188,899-49,196,208 SHC4
    nsv6959742copy number variation1nstd229human GRCh38 chr15: 48,876,169-48,879,507 , GRCh37.p13 chr15: 49,168,366-49,171,704 EID1, SHC4
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6623266copy number variation1nstd224human GRCh37 chr15: 49,251,367-49,627,694 , GRCh38.p12 chr15: 48,959,170-49,335,497 COPS2, RPL15P19, 9 more genes
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