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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5934882copy number variation1nstd209human GRCh38 chr15: 41,041,884-41,041,933 , GRCh37.p13 chr15: 41,334,082-41,334,131 INO80
    nsv5933156copy number variation1nstd209human GRCh38 chr15: 41,066,090-41,066,622 , GRCh37.p13 chr15: 41,358,288-41,358,820 INO80
    nsv5867135copy number variation1nstd209human GRCh38 chr15: 41,073,509-41,075,308 , GRCh37.p13 chr15: 41,365,707-41,367,506 INO80
    nsv5858858copy number variation1nstd209human GRCh38 chr15: 41,033,596-41,034,895 , GRCh37.p13 chr15: 41,325,794-41,327,093 INO80
    nsv5854938copy number variation1nstd209human GRCh38 chr15: 41,040,036-41,041,235 , GRCh37.p13 chr15: 41,332,234-41,333,433 INO80
    nsv5717897mobile element insertion1nstd211human GRCh38 chr15: 41,110,914-41,110,914 , GRCh37.p13 chr15: 41,403,112-41,403,112 INO80
    nsv5707994mobile element insertion2nstd211human GRCh38 chr15: 41,034,617-41,034,617 , GRCh37.p13 chr15: 41,326,815-41,326,815 INO80
    nsv5659828insertion1nstd207human GRCh38 chr15: 41,031,571-41,031,571 , GRCh37.p13 chr15: 41,323,769-41,323,769 INO80
    nsv5657975insertion2nstd207human GRCh38 chr15: 41,031,545-41,031,545 , GRCh37.p13 chr15: 41,323,743-41,323,743 INO80
    nsv5591997copy number variation1nstd207human GRCh38 chr15: 41,041,884-41,041,933 , GRCh37.p13 chr15: 41,334,082-41,334,131 INO80
    nsv5591669copy number variation1nstd207human GRCh38 chr15: 41,031,948-41,031,997 , GRCh37.p13 chr15: 41,324,146-41,324,195 INO80
    nsv5588030copy number variation1nstd207human GRCh38 chr15: 41,031,557-41,031,611 , GRCh37.p13 chr15: 41,323,755-41,323,809 INO80
    nsv5508892copy number variation1nstd206human GRCh38 chr15: 41,066,090-41,066,625 , GRCh37.p13 chr15: 41,358,288-41,358,823 INO80
    nsv5508471copy number variation1nstd206human GRCh38 chr15: 41,108,039-41,111,681 , GRCh37.p13 chr15: 41,400,237-41,403,879 CYCSP2, INO80
    nsv5502780copy number variation1nstd206human GRCh38 chr15: 41,109,980-41,111,401 , GRCh37.p13 chr15: 41,402,178-41,403,599 INO80
    nsv5501581copy number variation1nstd206human GRCh38 chr15: 41,059,039-41,059,212 , GRCh37.p13 chr15: 41,351,237-41,351,410 INO80
    nsv5499510copy number variation1nstd206human GRCh38 chr15: 41,059,193-41,059,248 , GRCh37.p13 chr15: 41,351,391-41,351,446 INO80
    nsv5498969copy number variation1nstd206human GRCh38 chr15: 41,007,560-41,007,665 , GRCh37.p13 chr15: 41,299,758-41,299,863 INO80
    nsv5426369mobile element insertion1nstd206human GRCh38 chr15: 41,034,617-41,034,668 , GRCh37.p13 chr15: 41,326,815-41,326,866 INO80
    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
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