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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974458insertion1nstd209human GRCh38 chr15: 66,469,693-66,469,693 , GRCh37.p13 chr15: 66,762,031-66,762,031 MAP2K1
    nsv5974378insertion1nstd209human GRCh38 chr15: 66,420,721-66,420,721 , GRCh37.p13 chr15: 66,713,059-66,713,059 MAP2K1
    nsv5942123copy number variation1nstd209human GRCh38 chr15: 66,389,625-66,398,801 , GRCh37.p13 chr15: 66,681,963-66,691,139 MAP2K1
    nsv5940500copy number variation1nstd209human GRCh38 chr15: 66,461,017-66,467,530 , GRCh37.p13 chr15: 66,753,355-66,759,868 MAP2K1
    nsv5935203copy number variation1nstd209human GRCh38 chr15: 66,414,198-66,414,344 , GRCh37.p13 chr15: 66,706,536-66,706,682 ATP5MFP6, MAP2K1
    nsv5864030copy number variation2nstd209human GRCh38 chr15: 66,389,716-66,390,715 , GRCh37.p13 chr15: 66,682,054-66,683,053 MAP2K1
    nsv5863794copy number variation2nstd209human GRCh38 chr15: 66,395,566-66,396,665 , GRCh37.p13 chr15: 66,687,904-66,689,003 MAP2K1
    nsv5858729copy number variation1nstd209human GRCh38 chr15: 66,461,073-66,467,597 , GRCh37.p13 chr15: 66,753,411-66,759,935 MAP2K1
    nsv5858537copy number variation1nstd209human GRCh38 chr15: 66,461,298-66,462,647 , GRCh37.p13 chr15: 66,753,636-66,754,985 MAP2K1
    nsv5857919copy number variation1nstd209human GRCh38 chr15: 66,389,604-66,398,818 , GRCh37.p13 chr15: 66,681,942-66,691,156 MAP2K1
    nsv5847703copy number variation1nstd209human GRCh38 chr15: 66,462,598-66,463,697 , GRCh37.p13 chr15: 66,754,936-66,756,035 MAP2K1
    nsv5711163mobile element insertion1nstd211human GRCh38 chr15: 66,469,499-66,469,499 , GRCh37.p13 chr15: 66,761,837-66,761,837 MAP2K1
    nsv5662984insertion1nstd207human GRCh38 chr15: 66,478,417-66,478,417 , GRCh37.p13 chr15: 66,770,755-66,770,755 MAP2K1
    nsv5660297insertion1nstd207human GRCh38 chr15: 66,420,779-66,420,779 , GRCh37.p13 chr15: 66,713,117-66,713,117 MAP2K1
    nsv5591869copy number variation1nstd207human GRCh38 chr15: 66,414,198-66,414,344 , GRCh37.p13 chr15: 66,706,536-66,706,682 ATP5MFP6, MAP2K1
    nsv5532976copy number variation1nstd206human GRCh38 chr15: 66,414,201-66,414,345 , GRCh37.p13 chr15: 66,706,539-66,706,683 MAP2K1, ATP5MFP6
    nsv5528937copy number variation1nstd206human GRCh38 chr15: 66,478,313-66,478,383 , GRCh37.p13 chr15: 66,770,651-66,770,721 MAP2K1
    nsv5389865copy number variation3nstd186human GRCh37 chr15: 66,706,539-66,706,683 , GRCh38.p12 chr15: 66,414,201-66,414,345 ATP5MFP6, MAP2K1
    nsv5380765copy number variation1nstd102humanUncertain significance GRCh37 chr15: 66,679,676-66,782,963 , GRCh38.p12 chr15: 66,387,338-66,490,625 MAP2K1, TIPIN, 3 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
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