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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099225copy number variation1nstd231human GRCh38.p12 chr1: 111,381,594-114,553,029 , GRCh37 chr1: 111,924,216-115,095,650 ADORA3, RHOC, 74 more genes
    nsv7095696copy number variation1nstd102humanPathogenic GRCh37 chr1: 112,318,699-115,576,848 , GRCh38.p12 chr1: 111,776,077-115,034,227 AKR7A2P1, PTPN22, 69 more genes
    nsv7095695copy number variation1nstd102humanPathogenic GRCh37 chr1: 111,145,905-114,454,813 , GRCh38.p12 chr1: 110,603,283-113,912,191 LOC107985189, RNU6-792P, 83 more genes
    nsv7048257inversion1nstd229human GRCh38 chr1: 111,787,369-111,787,487 , GRCh37.p13 chr1: 112,329,991-112,330,109 KCND3
    nsv6640096copy number variation1nstd229human GRCh38 chr1: 111,978,557-111,978,757 , GRCh37.p13 chr1: 112,521,179-112,521,379 KCND3
    nsv6640095copy number variation1nstd229human GRCh38 chr1: 111,959,167-111,962,946 , GRCh37.p13 chr1: 112,501,789-112,505,568 KCND3
    nsv6640094copy number variation1nstd229human GRCh38 chr1: 111,889,791-111,912,151 , GRCh37.p13 chr1: 112,432,413-112,454,773 KCND3, KCND3-AS1
    nsv6640092copy number variation1nstd229human GRCh38 chr1: 111,853,005-111,853,688 , GRCh37.p13 chr1: 112,395,627-112,396,310 KCND3, KCND3-IT1
    nsv6640090copy number variation1nstd229human GRCh38 chr1: 111,810,837-111,811,001 , GRCh37.p13 chr1: 112,353,459-112,353,623 KCND3
    nsv6640063copy number variation1nstd229human GRCh38 chr1: 111,888,801-111,892,500 , GRCh37.p13 chr1: 112,431,423-112,435,122 KCND3
    nsv6640062copy number variation1nstd229human GRCh38 chr1: 111,887,601-111,889,500 , GRCh37.p13 chr1: 112,430,223-112,432,122 KCND3
    nsv6640059copy number variation1nstd229human GRCh38 chr1: 111,871,499-111,882,850 , GRCh37.p13 chr1: 112,414,121-112,425,472 KCND3
    nsv6640058copy number variation1nstd229human GRCh38 chr1: 111,772,801-112,097,300 , GRCh37.p13 chr1: 112,315,423-112,639,922 LOC105378906, LINC01750, 3 more genes
    nsv6639965copy number variation1nstd229human GRCh38 chr1: 111,934,181-111,943,382 , GRCh37.p13 chr1: 112,476,803-112,486,004 KCND3
    nsv6639964copy number variation1nstd229human GRCh38 chr1: 111,900,279-111,904,737 , GRCh37.p13 chr1: 112,442,901-112,447,359 KCND3
    nsv6639626copy number variation1nstd229human GRCh38 chr1: 111,963,345-111,965,347 , GRCh37.p13 chr1: 112,505,967-112,507,969 KCND3
    nsv6639625copy number variation1nstd229human GRCh38 chr1: 111,887,701-111,889,600 , GRCh37.p13 chr1: 112,430,323-112,432,222 KCND3
    nsv6639624copy number variation1nstd229human GRCh38 chr1: 111,882,801-111,886,400 , GRCh37.p13 chr1: 112,425,423-112,429,022 KCND3
    nsv6639623copy number variation1nstd229human GRCh38 chr1: 111,858,975-111,859,408 , GRCh37.p13 chr1: 112,401,597-112,402,030 KCND3
    nsv6639621copy number variation1nstd229human GRCh38 chr1: 111,800,795-111,800,908 , GRCh37.p13 chr1: 112,343,417-112,343,530 KCND3
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