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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120938copy number variation1nstd186human GRCh37 chr10: 33,264,484-33,266,242 , GRCh38.p12 chr10: 32,975,556-32,977,314 ITGB1-DT
    nsv5927110copy number variation1nstd209human GRCh38 chr10: 32,994,272-32,994,333 , GRCh37.p13 chr10: 33,283,200-33,283,261 ITGB1-DT
    nsv5916457copy number variation1nstd209human GRCh38 chr10: 32,983,543-32,983,602 , GRCh37.p13 chr10: 33,272,471-33,272,530 ITGB1-DT
    nsv5914382copy number variation1nstd209human GRCh38 chr10: 27,312,316-36,846,398 , GRCh37.p13 chr10: 27,601,245-37,135,326 , RN7SL241P, 160 more genes
    nsv5914035copy number variation1nstd209human GRCh38 chr10: 33,050,275-33,050,376 , GRCh37.p13 chr10: 33,339,203-33,339,304 ITGB1-DT
    nsv5912468copy number variation1nstd209human GRCh38 chr10: 32,975,552-32,977,313 , GRCh37.p13 chr10: 33,264,480-33,266,241 ITGB1-DT
    nsv5851458copy number variation1nstd209human GRCh38 chr10: 32,975,491-32,977,290 , GRCh37.p13 chr10: 33,264,419-33,266,218 ITGB1-DT
    nsv5721467mobile element insertion2nstd211human GRCh38 chr10: 33,026,405-33,026,405 , GRCh37.p13 chr10: 33,315,333-33,315,333 ITGB1-DT
    nsv5706104mobile element insertion1nstd211human GRCh38 chr10: 32,983,565-32,983,565 , GRCh37.p13 chr10: 33,272,493-33,272,493 ITGB1-DT
    nsv5703266mobile element insertion1nstd211human GRCh38 chr10: 33,039,614-33,039,614 , GRCh37.p13 chr10: 33,328,542-33,328,542 ITGB1-DT
    nsv5642455insertion1nstd207human GRCh38 chr10: 33,026,392-33,026,392 , GRCh37.p13 chr10: 33,315,320-33,315,320 ITGB1-DT
    nsv5641452insertion1nstd207human GRCh38 chr10: 33,059,323-33,059,323 , GRCh37.p13 chr10: 33,348,251-33,348,251 ITGB1-DT
    nsv5589587copy number variation1nstd207human GRCh38 chr10: 32,975,552-32,977,313 , GRCh37.p13 chr10: 33,264,480-33,266,241 ITGB1-DT
    nsv5556101mobile element insertion1nstd206human GRCh38 chr10: 33,026,405-33,026,456 , GRCh37.p13 chr10: 33,315,333-33,315,384 ITGB1-DT
    nsv5490681copy number variation1nstd206human GRCh38 chr10: 32,975,556-32,977,314 , GRCh37.p13 chr10: 33,264,484-33,266,242 ITGB1-DT
    nsv5476006copy number variation1nstd206human GRCh38 chr10: 33,059,528-33,061,502 , GRCh37.p13 chr10: 33,348,456-33,350,430 ITGB1-DT
    nsv5411690mobile element insertion1nstd206human GRCh38 chr10: 32,983,565-32,983,616 , GRCh37.p13 chr10: 33,272,493-33,272,544 ITGB1-DT
    nsv5409480mobile element insertion1nstd206human GRCh38 chr10: 33,039,614-33,039,665 , GRCh37.p13 chr10: 33,328,542-33,328,593 ITGB1-DT
    nsv5354279translocation1nstd200human GRCh38 chr10: 33,002,394-33,002,394 , GRCh38 chr10: 33,002,470-33,002,470 , GRCh37.p13 chr10: 33,291,322-33,291,322 , GRCh37.p13 chr10: 33,291,398-33,291,398 ITGB1-DT
    nsv5354278translocation1nstd200human GRCh38 chr10: 32,975,556-32,975,556 , GRCh38 chr10: 32,977,314-32,977,314 , GRCh37.p13 chr10: 33,264,484-33,264,484 , GRCh37.p13 chr10: 33,266,242-33,266,242 ITGB1-DT
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