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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950281insertion1nstd209human GRCh38 chr1: 111,797,839-111,797,839 , GRCh37.p13 chr1: 112,340,461-112,340,461 KCND3
    nsv5882364copy number variation1nstd209human GRCh38 chr1: 111,889,787-111,912,145 , GRCh37.p13 chr1: 112,432,409-112,454,767 KCND3-AS1, KCND3
    nsv5827805copy number variation1nstd209human GRCh38 chr1: 111,889,766-111,904,628 , GRCh37.p13 chr1: 112,432,388-112,447,250 KCND3
    nsv5827715copy number variation1nstd209human GRCh38 chr1: 111,884,162-111,886,165 , GRCh37.p13 chr1: 112,426,784-112,428,787 KCND3
    nsv5723593mobile element insertion2nstd211human GRCh38 chr1: 111,797,854-111,797,854 , GRCh37.p13 chr1: 112,340,476-112,340,476 KCND3
    nsv5692088mobile element insertion1nstd211human GRCh38 chr1: 111,825,727-111,825,727 , GRCh37.p13 chr1: 112,368,349-112,368,349 KCND3
    nsv5674651mobile element insertion1nstd211human GRCh38 chr1: 111,818,925-111,818,925 , GRCh37.p13 chr1: 112,361,547-112,361,547 KCND3
    nsv5558911mobile element insertion1nstd206human GRCh38 chr1: 111,797,854-111,797,905 , GRCh37.p13 chr1: 112,340,476-112,340,527 KCND3
    nsv5543982insertion1nstd206human GRCh38 chr1: 111,793,475-111,793,475 , GRCh37.p13 chr1: 112,336,097-112,336,097 KCND3
    nsv5429360copy number variation1nstd206human GRCh38 chr1: 111,687,835-115,150,000 , GRCh37.p13 chr1: 112,230,457-115,692,621 , ST7L, 77 more genes
    nsv5422669copy number variation1nstd206human GRCh38 chr1: 111,799,411-111,817,008 , GRCh37.p13 chr1: 112,342,033-112,359,630 KCND3
    nsv5422179copy number variation1nstd206human GRCh38 chr1: 111,791,639-111,791,694 , GRCh37.p13 chr1: 112,334,261-112,334,316 KCND3
    nsv5394037mobile element insertion1nstd206human GRCh38 chr1: 111,825,727-111,825,778 , GRCh37.p13 chr1: 112,368,349-112,368,400 KCND3
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5284526copy number variation1nstd204human GRCh38.p13 chr1: 111,814,759-111,814,871 , GRCh37.p13 chr1: 112,357,381-112,357,493 KCND3
    nsv5196733mobile element insertion1nstd203human GRCh38 chr1: 111,797,840-111,797,849 , GRCh37.p13 chr1: 112,340,462-112,340,471 KCND3
    nsv5194424mobile element insertion1nstd203human GRCh38 chr1: 111,797,843-111,797,854 , GRCh37.p13 chr1: 112,340,465-112,340,476 KCND3
    nsv5192742mobile element insertion1nstd203human GRCh38 chr1: 111,797,839-111,797,854 , GRCh37.p13 chr1: 112,340,461-112,340,476 KCND3
    nsv5192563mobile element insertion1nstd203human GRCh38 chr1: 111,797,842-111,797,854 , GRCh37.p13 chr1: 112,340,464-112,340,476 KCND3
    nsv5188484mobile element insertion1nstd203human GRCh38 chr1: 111,797,846-111,797,849 , GRCh37.p13 chr1: 112,340,468-112,340,471 KCND3
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