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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5974367insertion1nstd209human GRCh38 chr18: 26,346,835-26,346,835 , GRCh37.p13 chr18: 23,926,799-23,926,799 TAF4B, LOC100419894
    nsv5968219insertion1nstd209human GRCh38 chr18: 26,285,222-26,285,222 , GRCh37.p13 chr18: 23,865,186-23,865,186 TAF4B
    nsv5943521copy number variation1nstd209human GRCh38 chr18: 26,346,855-26,346,906 , GRCh37.p13 chr18: 23,926,819-23,926,870 LOC100419894, TAF4B
    nsv5938906copy number variation1nstd209human GRCh38 chr18: 26,319,160-26,319,465 , GRCh37.p13 chr18: 23,899,124-23,899,429 TAF4B
    nsv5936351copy number variation1nstd209human GRCh38 chr18: 26,383,594-26,383,669 , GRCh37.p13 chr18: 23,963,558-23,963,633 TAF4B
    nsv5935617copy number variation1nstd209human GRCh38 chr18: 26,233,705-26,233,792 , GRCh37.p13 chr18: 23,813,669-23,813,756 TAF4B
    nsv5932791copy number variation1nstd209human GRCh38 chr18: 26,228,543-26,228,933 , GRCh37.p13 chr18: 23,808,507-23,808,897 TAF4B
    nsv5931294copy number variation1nstd209human GRCh38 chr18: 26,248,211-26,248,910 , GRCh37.p13 chr18: 23,828,175-23,828,874 TAF4B
    nsv5928348copy number variation1nstd209human GRCh38 chr18: 26,270,670-26,270,755 , GRCh37.p13 chr18: 23,850,634-23,850,719 TAF4B
    nsv5710639mobile element insertion2nstd211human GRCh38 chr18: 26,344,369-26,344,369 , GRCh37.p13 chr18: 23,924,333-23,924,333 TAF4B
    nsv5706889mobile element insertion1nstd211human GRCh38 chr18: 26,312,117-26,312,117 , GRCh37.p13 chr18: 23,892,081-23,892,081 TAF4B
    nsv5663829insertion1nstd207human GRCh38 chr18: 26,346,821-26,346,821 , GRCh37.p13 chr18: 23,926,785-23,926,785 TAF4B, LOC100419894
    nsv5601683copy number variation1nstd207human GRCh38 chr18: 26,247,842-26,248,490 , GRCh37.p13 chr18: 23,827,806-23,828,454 TAF4B
    nsv5590476copy number variation1nstd207human GRCh38 chr18: 26,346,799-26,346,856 , GRCh37.p13 chr18: 23,926,763-23,926,820 LOC100419894, TAF4B
    nsv5585629copy number variation1nstd207human GRCh38 chr18: 26,270,670-26,270,755 , GRCh37.p13 chr18: 23,850,634-23,850,719 TAF4B
    nsv5532074copy number variation1nstd206human GRCh38 chr18: 26,228,543-26,228,937 , GRCh37.p13 chr18: 23,808,507-23,808,901 TAF4B
    nsv5524740copy number variation1nstd206human GRCh38 chr18: 26,308,083-26,308,139 , GRCh37.p13 chr18: 23,888,047-23,888,103 TAF4B
    nsv5517019copy number variation1nstd206human GRCh38 chr18: 26,228,606-26,228,728 , GRCh37.p13 chr18: 23,808,570-23,808,692 TAF4B
    nsv5424327mobile element insertion1nstd206human GRCh38 chr18: 26,312,117-26,312,168 , GRCh37.p13 chr18: 23,892,081-23,892,132 TAF4B
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