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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5927477copy number variation1nstd209human GRCh38 chr7: 20,336,510-20,337,487 , GRCh37.p13 chr7: 20,376,133-20,377,110 ITGB8
    nsv5917335copy number variation1nstd209human GRCh38 chr7: 20,411,777-20,411,970 , GRCh37.p13 chr7: 20,451,400-20,451,593 ITGB8
    nsv5917306copy number variation1nstd209human GRCh38 chr7: 20,353,643-20,353,960 , GRCh37.p13 chr7: 20,393,266-20,393,583 ITGB8
    nsv5692091mobile element insertion2nstd211human GRCh38 chr7: 20,398,382-20,398,382 , GRCh37.p13 chr7: 20,438,005-20,438,005 ITGB8
    nsv5572702copy number variation1nstd207human GRCh38 chr7: 20,353,636-20,353,953 , GRCh37.p13 chr7: 20,393,259-20,393,576 ITGB8
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5546759insertion1nstd206human GRCh38 chr7: 20,398,382-20,398,433 , GRCh37.p13 chr7: 20,438,005-20,438,056 ITGB8
    nsv5467558copy number variation1nstd206human GRCh38 chr7: 20,411,780-20,411,971 , GRCh37.p13 chr7: 20,451,403-20,451,594 ITGB8
    nsv5465956copy number variation1nstd206human GRCh38 chr7: 20,354,450-20,357,177 , GRCh37.p13 chr7: 20,394,073-20,396,800 ITGB8
    nsv5456492copy number variation1nstd206human GRCh38 chr7: 20,339,047-20,339,845 , GRCh37.p13 chr7: 20,378,670-20,379,468 ITGB8
    nsv5382470mobile element deletion2nstd186human GRCh37 chr7: 20,393,274-20,393,577 , GRCh38.p12 chr7: 20,353,651-20,353,954 ITGB8
    nsv5370386translocation1nstd200human GRCh38 chr7: 20,341,922-20,341,922 , GRCh38 chr7: 20,341,852-20,341,852 , GRCh37.p13 chr7: 20,381,475-20,381,475 , GRCh37.p13 chr7: 20,381,545-20,381,545 ITGB8
    nsv5218487mobile element deletion1nstd204human GRCh38.p13 chr7: 20,353,643-20,353,958 , GRCh37.p13 chr7: 20,393,266-20,393,581 ITGB8
    nsv5119773mobile element insertion1nstd203human GRCh38 chr7: 20,398,368-20,398,382 , GRCh37.p13 chr7: 20,437,991-20,438,005 ITGB8
    nsv5107203mobile element insertion1nstd203human GRCh38 chr7: 20,389,291-20,389,291 , GRCh37.p13 chr7: 20,428,914-20,428,914 ITGB8
    nsv5100733mobile element insertion1nstd203human GRCh38 chr7: 20,366,401-20,366,416 , GRCh37.p13 chr7: 20,406,024-20,406,039 ITGB8
    nsv4955883copy number variation1nstd200human GRCh38 chr7: 20,411,780-20,411,971 , GRCh37.p13 chr7: 20,451,403-20,451,594 ITGB8
    nsv4955882copy number variation1nstd200human GRCh38 chr7: 20,348,289-20,354,568 , GRCh37.p13 chr7: 20,387,912-20,394,191 ITGB8
    nsv4953467copy number variation1nstd200human GRCh38 chr7: 20,405,750-20,420,415 , GRCh37.p13 chr7: 20,445,373-20,460,038 ITGB8
    nsv4953466copy number variation1nstd200human GRCh38 chr7: 20,347,439-20,654,167 , GRCh37.p13 chr7: 20,387,062-20,693,790 ITGB8, LOC402641, 2 more genes
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