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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922546copy number variation1nstd209human GRCh38 chr8: 17,104,697-17,105,018 , GRCh37.p13 chr8: 16,962,206-16,962,527 MICU3
    nsv5922107copy number variation1nstd209human GRCh38 chr8: 17,127,475-17,127,535 , GRCh37.p13 chr8: 16,984,984-16,985,044 MICU3
    nsv5713390mobile element insertion2nstd211human GRCh38 chr8: 17,107,542-17,107,542 , GRCh37.p13 chr8: 16,965,051-16,965,051 MICU3
    nsv5583590copy number variation1nstd207human GRCh38 chr8: 17,104,697-17,105,018 , GRCh37.p13 chr8: 16,962,206-16,962,527 MICU3
    nsv5582661copy number variation1nstd207human GRCh38 chr8: 17,127,475-17,127,535 , GRCh37.p13 chr8: 16,984,984-16,985,044 MICU3
    nsv5486481copy number variation1nstd206human GRCh38 chr8: 17,106,743-17,106,902 , GRCh37.p13 chr8: 16,964,252-16,964,411 MICU3
    nsv5485933copy number variation1nstd206human GRCh38 chr8: 17,127,480-17,127,536 , GRCh37.p13 chr8: 16,984,989-16,985,045 MICU3
    nsv5476897copy number variation1nstd206human GRCh38 chr8: 17,104,713-17,105,019 , GRCh37.p13 chr8: 16,962,222-16,962,528 MICU3
    nsv5411212mobile element insertion1nstd206human GRCh38 chr8: 17,107,542-17,107,593 , GRCh37.p13 chr8: 16,965,051-16,965,102 MICU3
    nsv5384644mobile element deletion2nstd186human GRCh37 chr8: 16,962,222-16,962,528 , GRCh38.p12 chr8: 17,104,713-17,105,019 MICU3
    nsv5379071translocation1nstd200human GRCh38 chr8: 17,127,536-17,127,536 , GRCh38 chr8: 17,127,480-17,127,480 , GRCh37.p13 chr8: 16,984,989-16,984,989 , GRCh37.p13 chr8: 16,985,045-16,985,045 MICU3
    nsv5379070translocation1nstd200human GRCh38 chr8: 17,035,311-17,035,311 , GRCh38 chr8: 17,036,869-17,036,869 , GRCh37.p13 chr8: 16,892,820-16,892,820 , GRCh37.p13 chr8: 16,894,378-16,894,378 MICU3
    nsv5344215translocation1nstd200human GRCh37 chr8: 16,985,045-16,985,045 , GRCh37 chr8: 16,984,989-16,984,989 , GRCh38.p12 chr8: 17,127,480-17,127,480 , GRCh38.p12 chr8: 17,127,536-17,127,536 MICU3
    nsv5337857translocation1nstd200human GRCh37 chr8: 16,943,530-16,943,530 , GRCh37 chr8: 16,943,366-16,943,366 , GRCh38.p12 chr8: 17,085,857-17,085,857 , GRCh38.p12 chr8: 17,086,021-17,086,021 MICU3
    nsv5322614translocation1nstd204human GRCh38.p13 chr8: 17,127,536-17,127,536 , GRCh38.p13 chr8: 17,127,480-17,127,480 , GRCh37.p13 chr8: 16,984,989-16,984,989 , GRCh37.p13 chr8: 16,985,045-16,985,045 MICU3
    nsv5242298copy number variation1nstd204human GRCh38.p13 chr8: 17,104,701-17,105,000 , GRCh37.p13 chr8: 16,962,210-16,962,509 MICU3
    nsv5201181mobile element deletion1nstd204human GRCh38.p13 chr8: 17,104,713-17,105,019 , GRCh37.p13 chr8: 16,962,222-16,962,528 MICU3
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5186791mobile element insertion1nstd203human GRCh38 chr8: 17,025,716-17,025,726 , GRCh37.p13 chr8: 16,883,225-16,883,235 MICU3
    nsv5119310mobile element insertion1nstd203human GRCh38 chr8: 17,107,527-17,107,542 , GRCh37.p13 chr8: 16,965,036-16,965,051 MICU3
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