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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919260copy number variation1nstd209human GRCh38 chr10: 75,144,296-75,144,526 , GRCh37.p13 chr10: 76,904,054-76,904,284 SAMD8
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5716883mobile element insertion1nstd211human GRCh38 chr10: 75,165,291-75,165,291 , GRCh37.p13 chr10: 76,925,049-76,925,049 SAMD8
    nsv5712177mobile element insertion1nstd211human GRCh38 chr10: 75,155,207-75,155,207 , GRCh37.p13 chr10: 76,914,965-76,914,965 SAMD8
    nsv5638109insertion1nstd207human GRCh38 chr10: 75,135,836-75,135,836 , GRCh37.p13 chr10: 76,895,594-76,895,594 SAMD8
    nsv5597416copy number variation1nstd207human GRCh38 chr10: 75,144,296-75,144,526 , GRCh37.p13 chr10: 76,904,054-76,904,284 SAMD8
    nsv5560551mobile element insertion1nstd206human GRCh38 chr10: 75,165,291-75,165,342 , GRCh37.p13 chr10: 76,925,049-76,925,100 SAMD8
    nsv5487358copy number variation1nstd206human GRCh38 chr10: 75,128,773-75,135,890 , GRCh37.p13 chr10: 76,888,531-76,895,648 SAMD8
    nsv5482833copy number variation1nstd206human GRCh38 chr10: 75,116,096-75,116,286 , GRCh37.p13 chr10: 76,875,854-76,876,044 SAMD8
    nsv5482359copy number variation1nstd206human GRCh38 chr10: 75,164,794-75,165,370 , GRCh37.p13 chr10: 76,924,552-76,925,128 SAMD8
    nsv5477783copy number variation1nstd206human GRCh38 chr10: 75,144,297-75,144,527 , GRCh37.p13 chr10: 76,904,055-76,904,285 SAMD8
    nsv5476299copy number variation1nstd206human GRCh38 chr10: 75,174,363-75,174,418 , GRCh37.p13 chr10: 76,934,121-76,934,176 SAMD8
    nsv5402533mobile element insertion1nstd206human GRCh38 chr10: 75,155,207-75,155,258 , GRCh37.p13 chr10: 76,914,965-76,915,016 SAMD8
    nsv5373265translocation1nstd200human GRCh38 chr10: 75,164,794-75,164,794 , GRCh38 chr10: 75,165,370-75,165,370 , GRCh37.p13 chr10: 76,925,128-76,925,128 , GRCh37.p13 chr10: 76,924,552-76,924,552 SAMD8
    nsv5367798translocation1nstd200human GRCh38 chr10: 75,181,081-75,181,081 , GRCh38 chr4: 121,601,128-121,601,128 , GRCh37.p13 chr10: 76,940,839-76,940,839 , GRCh37.p13 chr4: 122,522,283-122,522,283 SAMD8
    nsv5367797translocation1nstd200human GRCh38 chr4: 121,601,108-121,601,108 , GRCh38 chr10: 75,182,103-75,182,103 , GRCh37.p13 chr4: 122,522,263-122,522,263 , GRCh37.p13 chr10: 76,941,861-76,941,861 SAMD8
    nsv5347864translocation1nstd200human GRCh38 chr10: 75,144,527-75,144,527 , GRCh38 chr10: 75,144,297-75,144,297 , GRCh37.p13 chr10: 76,904,055-76,904,055 , GRCh37.p13 chr10: 76,904,285-76,904,285 SAMD8
    nsv5344809translocation1nstd200human GRCh37 chr10: 76,904,055-76,904,055 , GRCh37 chr10: 76,904,285-76,904,285 , GRCh38.p12 chr10: 75,144,527-75,144,527 , GRCh38.p12 chr10: 75,144,297-75,144,297 SAMD8
    nsv5030983inversion1nstd200human GRCh38 chr10: 75,143,067-75,148,840 , GRCh37.p13 chr10: 76,902,825-76,908,598 SAMD8
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
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