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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131225insertion1nstd186human GRCh37 chr17: 61,731,675-61,731,675 , GRCh38.p12 chr17: 63,654,315-63,654,315 MAP3K3
    nsv6128909copy number variation1nstd186human GRCh37 chr17: 61,731,528-61,731,675 , GRCh38.p12 chr17: 63,654,168-63,654,315 MAP3K3
    nsv5978619insertion1nstd209human GRCh38 chr17: 63,654,315-63,654,315 , GRCh37.p13 chr17: 61,731,675-61,731,675 MAP3K3
    nsv5972882insertion1nstd209human GRCh38 chr17: 63,668,005-63,668,005 , GRCh37.p13 chr17: 61,745,365-61,745,365 MAP3K3
    nsv5944431copy number variation1nstd209human GRCh38 chr17: 63,654,160-63,654,307 , GRCh37.p13 chr17: 61,731,520-61,731,667 MAP3K3
    nsv5929218copy number variation1nstd209human GRCh38 chr17: 63,672,102-63,674,385 , GRCh37.p13 chr17: 61,749,462-61,751,745 , MAP3K3
    nsv5887293copy number variation1nstd209human GRCh38 chr17: 63,672,128-63,674,427 , GRCh37.p13 chr17: 61,749,488-61,751,787 , MAP3K3
    nsv5700076mobile element insertion2nstd211human GRCh38 chr17: 63,654,333-63,654,333 , GRCh37.p13 chr17: 61,731,693-61,731,693 MAP3K3
    nsv5694407mobile element insertion2nstd211human GRCh38 chr17: 63,668,021-63,668,021 , GRCh37.p13 chr17: 61,745,381-61,745,381 MAP3K3
    nsv5660430insertion1nstd207human GRCh38 chr17: 63,654,315-63,654,315 , GRCh37.p13 chr17: 61,731,675-61,731,675 MAP3K3
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5550271insertion1nstd206human GRCh38 chr17: 63,654,315-63,654,315 , GRCh37.p13 chr17: 61,731,675-61,731,675 MAP3K3
    nsv5532110copy number variation1nstd206human GRCh38 chr17: 63,678,204-63,678,550 , GRCh37.p13 chr17: 61,755,564-61,755,910 , MAP3K3
    nsv5531701copy number variation1nstd206human GRCh38 chr17: 63,661,115-63,662,727 , GRCh37.p13 chr17: 61,738,475-61,740,087 MAP3K3
    nsv5526034copy number variation1nstd206human GRCh38 chr17: 63,654,168-63,654,315 , GRCh37.p13 chr17: 61,731,528-61,731,675 MAP3K3
    nsv5517484copy number variation1nstd206human GRCh38 chr17: 63,672,117-63,674,376 , GRCh37.p13 chr17: 61,749,477-61,751,736 , MAP3K3
    nsv5516704copy number variation1nstd206human GRCh38 chr17: 63,637,934-63,644,038 , GRCh37.p13 chr17: 61,715,294-61,721,398 MAP3K3
    nsv5417820mobile element insertion1nstd206human GRCh38 chr17: 63,668,021-63,668,072 , GRCh37.p13 chr17: 61,745,381-61,745,432 MAP3K3
    nsv5382280mobile element deletion1nstd186human GRCh37 chr17: 61,740,034-61,740,363 , GRCh38.p12 chr17: 63,662,674-63,663,003 MAP3K3
    nsv5359015translocation1nstd200human GRCh38 chr17: 63,678,204-63,678,204 , GRCh38 chr17: 63,678,550-63,678,550 , GRCh37.p13 chr17: 61,755,564-61,755,564 , GRCh37.p13 chr17: 61,755,910-61,755,910 , MAP3K3
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