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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5947394copy number variation1nstd209human GRCh38 chr12: 122,021,404-122,021,584 , GRCh37.p13 chr12: 122,459,310-122,459,490 BCL7A
    nsv5947089copy number variation1nstd209human GRCh38 chr12: 122,025,128-122,025,219 , GRCh37.p13 chr12: 122,463,034-122,463,125 BCL7A
    nsv5946967copy number variation1nstd209human GRCh38 chr12: 122,024,784-122,025,323 , GRCh37.p13 chr12: 122,462,690-122,463,229 BCL7A
    nsv5939885copy number variation1nstd209human GRCh38 chr12: 122,023,642-122,023,759 , GRCh37.p13 chr12: 122,461,548-122,461,665 BCL7A
    nsv5931663copy number variation1nstd209human GRCh38 chr12: 122,045,131-122,047,273 , GRCh37.p13 chr12: 122,483,037-122,485,179 BCL7A
    nsv5931554copy number variation1nstd209human GRCh38 chr12: 122,039,112-122,040,349 , GRCh37.p13 chr12: 122,477,018-122,478,255 BCL7A
    nsv5848432copy number variation1nstd209human GRCh38 chr12: 122,045,082-122,047,233 , GRCh37.p13 chr12: 122,482,988-122,485,139 BCL7A
    nsv5512532copy number variation1nstd206human GRCh38 chr12: 122,039,086-122,040,418 , GRCh37.p13 chr12: 122,476,992-122,478,324 BCL7A
    nsv5508301copy number variation1nstd206human GRCh38 chr12: 122,022,458-122,023,375 , GRCh37.p13 chr12: 122,460,364-122,461,281 BCL7A
    nsv5508031copy number variation1nstd206human GRCh38 chr12: 122,024,138-122,024,895 , GRCh37.p13 chr12: 122,462,044-122,462,801 BCL7A
    nsv5501839copy number variation1nstd206human GRCh38 chr12: 122,020,957-122,021,033 , GRCh37.p13 chr12: 122,458,863-122,458,939 BCL7A
    nsv5500383copy number variation1nstd206human GRCh38 chr12: 122,024,153-122,024,363 , GRCh37.p13 chr12: 122,462,059-122,462,269 BCL7A
    nsv5498155copy number variation1nstd206human GRCh38 chr12: 122,023,716-122,023,847 , GRCh37.p13 chr12: 122,461,622-122,461,753 BCL7A
    nsv5496329copy number variation1nstd206human GRCh38 chr12: 122,045,162-122,047,281 , GRCh37.p13 chr12: 122,483,068-122,485,187 BCL7A
    nsv5356467translocation1nstd200human GRCh38 chr12: 122,023,716-122,023,716 , GRCh38 chr12: 122,023,847-122,023,847 , GRCh37.p13 chr12: 122,461,753-122,461,753 , GRCh37.p13 chr12: 122,461,622-122,461,622 BCL7A
    nsv5343373translocation1nstd200human GRCh37 chr12: 122,461,622-122,461,622 , GRCh37 chr12: 122,461,753-122,461,753 , GRCh38.p12 chr12: 122,023,716-122,023,716 , GRCh38.p12 chr12: 122,023,847-122,023,847 BCL7A
    nsv5329008translocation1nstd204human GRCh38.p13 chr12: 122,023,847-122,023,847 , GRCh38.p13 chr12: 122,023,716-122,023,716 , GRCh37.p13 chr12: 122,461,622-122,461,622 , GRCh37.p13 chr12: 122,461,753-122,461,753 BCL7A
    nsv5305642copy number variation1nstd204human GRCh38.p13 chr12: 122,045,131-122,047,273 , GRCh37.p13 chr12: 122,483,037-122,485,179 BCL7A
    nsv4996090copy number variation1nstd200human GRCh38 chr12: 122,045,158-122,045,832 , GRCh37.p13 chr12: 122,483,064-122,483,738 BCL7A
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