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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925727copy number variation1nstd209human GRCh38 chr8: 1,776,265-1,776,488 , GRCh37.p13 chr8: 1,724,431-1,724,654 CLN8
    nsv5858754copy number variation1nstd209human GRCh38 chr8: 1,785,965-1,798,212 , GRCh37.p13 chr8: 1,734,131-1,746,378 CLN8
    nsv5638527insertion1nstd207human GRCh38 chr8: 1,763,601-1,763,601 , GRCh37.p13 chr8: 1,711,767-1,711,767 CLN8-AS1, CLN8
    nsv5636055insertion1nstd207human GRCh38 chr8: 1,776,008-1,776,008 , GRCh37.p13 chr8: 1,724,174-1,724,174 CLN8
    nsv5580960copy number variation1nstd207human GRCh38 chr8: 1,763,446-1,763,621 , GRCh37.p13 chr8: 1,711,612-1,711,787 CLN8, CLN8-AS1
    nsv5579694copy number variation1nstd207human GRCh38 chr8: 1,785,527-1,785,661 , GRCh37.p13 chr8: 1,733,693-1,733,827 CLN8
    nsv5575983copy number variation1nstd207human GRCh38 chr8: 1,763,389-1,763,473 , GRCh37.p13 chr8: 1,711,555-1,711,639 CLN8-AS1, CLN8
    nsv5556983sequence alteration1nstd206human GRCh38 chr8: 1,572,428-3,114,153 , GRCh37.p13 chr8: 1,520,594-2,971,675 , CLN8, 23 more genes
    nsv5479588copy number variation1nstd206human GRCh38 chr8: 1,771,913-1,772,528 , GRCh37.p13 chr8: 1,720,079-1,720,694 CLN8
    nsv5479437copy number variation1nstd206human GRCh38 chr8: 1,760,185-1,760,267 , GRCh37.p13 chr8: 1,708,351-1,708,433 CLN8-AS1, CLN8
    nsv5476432copy number variation1nstd206human GRCh38 chr8: 1,733,963-1,805,616 , GRCh37.p13 chr8: 1,682,129-1,753,782 CLN8, CLN8-AS1, 2 more genes
    nsv5371488translocation1nstd200human GRCh38 chr8: 1,786,155-1,786,155 , GRCh38 chr8: 1,784,693-1,784,693 , GRCh37.p13 chr8: 1,732,859-1,732,859 , GRCh37.p13 chr8: 1,734,321-1,734,321 CLN8
    nsv5371487translocation1nstd200human GRCh38 chr8: 1,785,779-1,785,779 , GRCh38 chr8: 1,784,691-1,784,691 , GRCh37.p13 chr8: 1,732,857-1,732,857 , GRCh37.p13 chr8: 1,733,945-1,733,945 CLN8
    nsv5309137copy number variation1nstd204human GRCh38.p13 chr8: 1,661,125-2,486,879 , GRCh37.p13 chr8: 1,609,291-2,343,985 , KBTBD11, 18 more genes
    nsv5255888copy number variation1nstd204human GRCh38.p13 chr8: 1,732,103-1,779,362 , GRCh37.p13 chr8: 1,680,269-1,727,528 LOC105377778, CLN8-AS1, 1 more genes
    nsv5251456copy number variation1nstd204human GRCh38.p13 chr8: 1,761,237-1,764,913 , GRCh37.p13 chr8: 1,709,403-1,713,079 CLN8-AS1, CLN8
    nsv5244405copy number variation1nstd204human GRCh38.p13 chr8: 1,735,001-2,235,500 , GRCh37.p13 chr8: 1,683,167-1,965,389 KBTBD11-AS1, LOC100131395, 13 more genes
    nsv5216482mobile element deletion1nstd204human GRCh38.p13 chr8: 1,766,378-1,766,700 , GRCh37.p13 chr8: 1,714,544-1,714,866 CLN8
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5113516mobile element insertion1nstd203human GRCh38 chr8: 1,765,545-1,765,560 , GRCh37.p13 chr8: 1,713,711-1,713,726 CLN8
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