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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978403insertion1nstd209human GRCh38 chr11: 43,855,889-43,855,889 , GRCh37.p13 chr11: 43,877,439-43,877,439 HSD17B12
    nsv5971550insertion1nstd209human GRCh38 chr11: 43,690,389-43,690,389 , GRCh37.p13 chr11: 43,711,939-43,711,939 HSD17B12
    nsv5968003insertion1nstd209human GRCh38 chr11: 43,590,457-43,590,457 , GRCh37.p13 chr11: 43,612,007-43,612,007 HSD17B12
    nsv5921579copy number variation1nstd209human GRCh38 chr11: 43,770,809-43,770,909 , GRCh37.p13 chr11: 43,792,359-43,792,459 HSD17B12
    nsv5915723copy number variation1nstd209human GRCh38 chr11: 43,694,027-43,695,061 , GRCh37.p13 chr11: 43,715,577-43,716,611 HSD17B12
    nsv5865144copy number variation1nstd209human GRCh38 chr11: 43,775,468-43,778,772 , GRCh37.p13 chr11: 43,797,018-43,800,322 HSD17B12
    nsv5729698mobile element insertion1nstd211human GRCh38 chr11: 43,691,737-43,691,737 , GRCh37.p13 chr11: 43,713,287-43,713,287 HSD17B12
    nsv5724170mobile element insertion1nstd211human GRCh38 chr11: 43,775,482-43,775,482 , GRCh37.p13 chr11: 43,797,032-43,797,032 HSD17B12
    nsv5723919mobile element insertion1nstd211human GRCh38 chr11: 43,671,591-43,671,591 , GRCh37.p13 chr11: 43,693,141-43,693,141 HSD17B12
    nsv5717361mobile element insertion1nstd211human GRCh38 chr11: 43,668,696-43,668,696 , GRCh37.p13 chr11: 43,690,246-43,690,246 HSD17B12
    nsv5706728mobile element insertion2nstd211human GRCh38 chr11: 43,803,869-43,803,869 , GRCh37.p13 chr11: 43,825,419-43,825,419 HSD17B12
    nsv5704928mobile element insertion1nstd211human GRCh38 chr11: 43,794,667-43,794,667 , GRCh37.p13 chr11: 43,816,217-43,816,217 HSD17B12
    nsv5704853mobile element insertion1nstd211human GRCh38 chr11: 43,741,029-43,741,029 , GRCh37.p13 chr11: 43,762,579-43,762,579 HSD17B12
    nsv5701313mobile element insertion1nstd211human GRCh38 chr11: 43,814,212-43,814,212 , GRCh37.p13 chr11: 43,835,762-43,835,762 HSD17B12
    nsv5697461mobile element insertion2nstd211human GRCh38 chr11: 43,641,084-43,641,084 , GRCh37.p13 chr11: 43,662,634-43,662,634 HSD17B12
    nsv5694788mobile element insertion2nstd211human GRCh38 chr11: 43,855,898-43,855,898 , GRCh37.p13 chr11: 43,877,448-43,877,448 HSD17B12
    nsv5663955insertion1nstd207human GRCh38 chr11: 43,855,889-43,855,889 , GRCh37.p13 chr11: 43,877,439-43,877,439 HSD17B12
    nsv5651598insertion1nstd207human GRCh38 chr11: 43,619,213-43,619,213 , GRCh37.p13 chr11: 43,640,763-43,640,763 HSD17B12
    nsv5646712insertion1nstd207human GRCh38 chr11: 43,641,069-43,641,069 , GRCh37.p13 chr11: 43,662,619-43,662,619 HSD17B12
    nsv5602118copy number variation1nstd207human GRCh38 chr11: 43,816,998-43,817,049 , GRCh37.p13 chr11: 43,838,548-43,838,599 HSD17B12
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