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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5916212copy number variation1nstd209human GRCh38 chr8: 81,762,550-81,846,688 , GRCh37.p13 chr8: 82,674,785-82,758,923 SNX16, HNRNPA1P36
    nsv5861364copy number variation1nstd209human GRCh38 chr8: 81,762,205-81,810,372 , GRCh37.p13 chr8: 82,674,440-82,722,607 SNX16, HNRNPA1P36
    nsv5860788copy number variation2nstd209human GRCh38 chr8: 81,816,773-81,818,072 , GRCh37.p13 chr8: 82,729,008-82,730,307 SNX16
    nsv5710324mobile element insertion2nstd211human GRCh38 chr8: 81,813,304-81,813,304 , GRCh37.p13 chr8: 82,725,539-82,725,539 SNX16
    nsv5641879insertion1nstd207human GRCh38 chr8: 81,842,539-81,842,539 , GRCh37.p13 chr8: 82,754,774-82,754,774 SNX16
    nsv5566180copy number variation1nstd207human GRCh38 chr8: 81,842,449-81,842,560 , GRCh37.p13 chr8: 82,754,684-82,754,795 SNX16
    nsv5564979copy number variation1nstd207human GRCh38 chr8: 81,842,534-81,842,583 , GRCh37.p13 chr8: 82,754,769-82,754,818 SNX16
    nsv5540590insertion1nstd206human GRCh38 chr8: 81,822,974-81,823,015 , GRCh37.p13 chr8: 82,735,209-82,735,250 SNX16
    nsv5492936copy number variation1nstd206human GRCh38 chr8: 81,842,384-81,842,515 , GRCh37.p13 chr8: 82,754,619-82,754,750 SNX16
    nsv5477272copy number variation1nstd206human GRCh38 chr8: 81,822,931-81,822,984 , GRCh37.p13 chr8: 82,735,166-82,735,219 SNX16
    nsv5410652mobile element insertion1nstd206human GRCh38 chr8: 81,813,304-81,813,355 , GRCh37.p13 chr8: 82,725,539-82,725,590 SNX16
    nsv5371889translocation1nstd200human GRCh38 chr8: 81,800,733-81,800,733 , GRCh38 chr8: 81,801,039-81,801,039 , GRCh37.p13 chr8: 82,713,274-82,713,274 , GRCh37.p13 chr8: 82,712,968-82,712,968 SNX16
    nsv5364132translocation1nstd200human GRCh38 chr8: 81,842,384-81,842,384 , GRCh38 chr8: 41,425,326-41,425,326 , GRCh37.p13 chr8: 82,754,619-82,754,619 , GRCh37.p13 chr8: 41,282,845-41,282,845 SNX16, SNORD65B
    nsv5347311translocation1nstd200human GRCh38 chr8: 81,842,384-81,842,384 , GRCh38 chr16: 87,202,970-87,202,970 , GRCh37.p13 chr16: 87,236,576-87,236,576 , GRCh37.p13 chr8: 82,754,619-82,754,619 SNX16
    nsv5347310translocation1nstd200human GRCh38 chr10: 114,927,163-114,927,163 , GRCh38 chr8: 81,842,384-81,842,384 , GRCh37.p13 chr8: 82,754,619-82,754,619 , GRCh37.p13 chr10: 116,686,922-116,686,922 SNX16
    nsv5334140translocation1nstd200human GRCh37 chr8: 82,712,968-82,712,968 , GRCh37 chr8: 82,713,274-82,713,274 , GRCh38.p12 chr8: 81,800,733-81,800,733 , GRCh38.p12 chr8: 81,801,039-81,801,039 SNX16
    nsv5259532copy number variation1nstd204human GRCh38.p13 chr8: 81,800,901-81,803,700 , GRCh37.p13 chr8: 82,713,136-82,715,935 SNX16
    nsv5256979copy number variation1nstd204human GRCh38.p13 chr8: 81,799,201-81,801,600 , GRCh37.p13 chr8: 82,711,436-82,713,835 SNX16
    nsv5250428copy number variation1nstd204human GRCh38.p13 chr8: 81,798,601-81,804,800 , GRCh37.p13 chr8: 82,710,836-82,717,035 SNX16
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
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