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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6113539mobile element insertion1nstd186human GRCh37 chr20: 52,637,949-52,638,000 , GRCh38.p12 chr20: 54,021,410-54,021,461 BCAS1
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5974158insertion1nstd209human GRCh38 chr20: 54,021,397-54,021,397 , GRCh37.p13 chr20: 52,637,936-52,637,936 BCAS1
    nsv5969523insertion1nstd209human GRCh38 chr20: 54,041,862-54,041,862 , GRCh37.p13 chr20: 52,658,401-52,658,401 BCAS1
    nsv5962453copy number variation1nstd209human GRCh38 chr20: 54,030,525-54,041,462 , GRCh37.p13 chr20: 52,647,064-52,658,001 BCAS1
    nsv5956701copy number variation1nstd209human GRCh38 chr20: 53,983,387-53,983,469 , GRCh37.p13 chr20: 52,599,926-52,600,008 BCAS1
    nsv5879761copy number variation1nstd209human GRCh38 chr20: 54,030,523-54,041,390 , GRCh37.p13 chr20: 52,647,062-52,657,929 BCAS1
    nsv5702785mobile element insertion1nstd211human GRCh38 chr20: 53,950,949-53,950,949 , GRCh37.p13 chr20: 52,567,488-52,567,488 BCAS1
    nsv5699276mobile element insertion1nstd211human GRCh38 chr20: 53,986,507-53,986,507 , GRCh37.p13 chr20: 52,603,046-52,603,046 BCAS1
    nsv5694789mobile element insertion2nstd211human GRCh38 chr20: 54,021,410-54,021,410 , GRCh37.p13 chr20: 52,637,949-52,637,949 BCAS1
    nsv5668522insertion1nstd207human GRCh38 chr20: 54,021,397-54,021,397 , GRCh37.p13 chr20: 52,637,936-52,637,936 BCAS1
    nsv5599359copy number variation1nstd207human GRCh38 chr20: 54,030,525-54,041,462 , GRCh37.p13 chr20: 52,647,064-52,658,001 BCAS1
    nsv5546476insertion1nstd206human GRCh38 chr20: 53,950,949-53,950,984 , GRCh37.p13 chr20: 52,567,488-52,567,523 BCAS1
    nsv5532487copy number variation1nstd206human GRCh38 chr20: 54,021,138-54,026,232 , GRCh37.p13 chr20: 52,637,677-52,642,771 BCAS1
    nsv5530165copy number variation1nstd206human GRCh38 chr20: 54,030,531-54,041,463 , GRCh37.p13 chr20: 52,647,070-52,658,002 BCAS1
    nsv5526484copy number variation1nstd206human GRCh38 chr20: 54,027,113-54,027,895 , GRCh37.p13 chr20: 52,643,652-52,644,434 BCAS1
    nsv5515640copy number variation1nstd206human GRCh38 chr20: 53,983,388-53,983,470 , GRCh37.p13 chr20: 52,599,927-52,600,009 BCAS1
    nsv5430833mobile element insertion1nstd206human GRCh38 chr20: 53,986,507-53,986,558 , GRCh37.p13 chr20: 52,603,046-52,603,097 BCAS1
    nsv5426297mobile element insertion1nstd206human GRCh38 chr20: 54,021,410-54,021,461 , GRCh37.p13 chr20: 52,637,949-52,638,000 BCAS1
    nsv5344567translocation1nstd200human GRCh37 chr20: 52,650,331-52,650,331 , GRCh37 chr20: 52,651,389-52,651,389 , GRCh38.p12 chr20: 54,033,792-54,033,792 , GRCh38.p12 chr20: 54,034,850-54,034,850 BCAS1
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