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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959074insertion1nstd209human GRCh38 chr6: 109,660,399-109,660,399 , GRCh37.p13 chr6: 109,981,602-109,981,602 AK9
    nsv5893680copy number variation1nstd209human GRCh38 chr6: 109,687,389-109,693,754 , GRCh37.p13 chr6: 110,008,592-110,014,957 FIG4, AK9
    nsv5891337copy number variation1nstd209human GRCh38 chr6: 109,644,468-109,644,538 , GRCh37.p13 chr6: 109,965,671-109,965,741 AK9
    nsv5843990copy number variation1nstd209human GRCh38 chr6: 109,687,629-109,693,728 , GRCh37.p13 chr6: 110,008,832-110,014,931 FIG4, AK9
    nsv5721497mobile element insertion1nstd211human GRCh38 chr6: 109,605,315-109,605,315 , GRCh37.p13 chr6: 109,926,518-109,926,518 AK9
    nsv5690319mobile element insertion2nstd211human GRCh38 chr6: 109,576,437-109,576,437 , GRCh37.p13 chr6: 109,897,640-109,897,640 AK9
    nsv5643801insertion1nstd207human GRCh38 chr6: 109,651,243-109,651,243 , GRCh37.p13 chr6: 109,972,446-109,972,446 AK9
    nsv5633320insertion1nstd207human GRCh38 chr6: 109,540,152-109,540,152 , GRCh37.p13 chr6: 109,861,355-109,861,355 AK9
    nsv5632961insertion1nstd207human GRCh38 chr6: 109,644,468-109,644,468 , GRCh37.p13 chr6: 109,965,671-109,965,671 AK9
    nsv5564516copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,796,301-113,083,437 , GRCh38.p12 chr6: 109,475,098-112,762,235 RN7SL617P, METTL24, 67 more genes
    nsv5558437mobile element insertion1nstd206human GRCh38 chr6: 109,605,315-109,605,366 , GRCh37.p13 chr6: 109,926,518-109,926,569 AK9
    nsv5552793insertion1nstd206human GRCh38 chr6: 109,592,108-109,592,108 , GRCh37.p13 chr6: 109,913,311-109,913,311 AK9
    nsv5473152copy number variation1nstd206human GRCh38 chr6: 109,629,542-109,629,663 , GRCh37.p13 chr6: 109,950,745-109,950,866 AK9
    nsv5470808copy number variation1nstd206human GRCh38 chr6: 109,648,343-109,651,672 , GRCh37.p13 chr6: 109,969,546-109,972,875 AK9
    nsv5465699copy number variation1nstd206human GRCh38 chr6: 109,564,870-109,564,932 , GRCh37.p13 chr6: 109,886,073-109,886,135 AK9
    nsv5458290copy number variation1nstd206human GRCh38 chr6: 109,644,468-109,644,543 , GRCh37.p13 chr6: 109,965,671-109,965,746 AK9
    nsv5394067mobile element insertion1nstd206human GRCh38 chr6: 109,575,712-109,575,763 , GRCh37.p13 chr6: 109,896,915-109,896,966 AK9
    nsv5343675translocation1nstd200human GRCh37 chr6: 109,824,428-109,824,428 , GRCh37 chr6: 109,824,179-109,824,179 , GRCh38.p12 chr6: 109,503,225-109,503,225 , GRCh38.p12 chr6: 109,502,976-109,502,976 AK9
    nsv5230208copy number variation1nstd204human GRCh38.p13 chr6: 109,668,601-109,669,000 , GRCh37.p13 chr6: 109,989,804-109,990,203 AK9
    nsv5222023copy number variation1nstd204human GRCh38.p13 chr6: 109,622,201-109,622,700 , GRCh37.p13 chr6: 109,943,404-109,943,903 AK9
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