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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5881509copy number variation1nstd209human GRCh38 chr1: 1,264,791-1,546,719 , GRCh37.p13 chr1: 1,200,171-1,482,099 , MRPL20-AS1, 30 more genes
    nsv5875894copy number variation1nstd209human GRCh38 chr1: 1,405,572-1,423,930 , GRCh37.p13 chr1: 1,340,952-1,359,310 , MRPL20, 3 more genes
    nsv5828187copy number variation1nstd209human GRCh38 chr1: 1,405,543-1,416,235 , GRCh37.p13 chr1: 1,340,923-1,351,615 , MRPL20, 1 more genes
    nsv5828185copy number variation1nstd209human GRCh38 chr1: 1,382,943-1,401,341 , GRCh37.p13 chr1: 1,318,323-1,336,721 MRPL20, CCNL2, 1 more genes
    nsv5281165copy number variation1nstd204human GRCh37.p13 chr1: 1,332,291-1,338,855 , GRCh38.p13 chr1: 1,396,911-1,403,475 MRPL20, CCNL2, 2 more genes
    nsv5214195copy number variation1nstd204human GRCh38.p13 chr1: 1,396,101-1,403,600 , GRCh37.p13 chr1: 1,331,481-1,338,980 CCNL2, MRPL20-AS1, 2 more genes
    nsv5213342copy number variation1nstd204human GRCh38.p13 chr1: 1,351,401-1,466,800 , GRCh37.p13 chr1: 1,286,781-1,402,180 , LINC01770, 13 more genes
    nsv5208305copy number variation1nstd204human GRCh38.p13 chr1: 890,901-1,634,500 , GRCh37.p13 chr1: 826,281-1,569,876 , PLEKHN1, 62 more genes
    nsv5206014copy number variation1nstd204human GRCh38.p13 chr1: 1,397,350-1,403,741 , GRCh37.p13 chr1: 1,332,730-1,339,121 MRPL20, CCNL2, 2 more genes
    nsv5199477mobile element insertion1nstd203human GRCh38 chr1: 1,405,913-1,405,928 , GRCh37.p13 chr1: 1,341,293-1,341,308 RN7SL657P, MRPL20
    nsv5072560mobile element insertion1nstd203human GRCh38 chr1: 1,403,968-1,403,968 , GRCh37.p13 chr1: 1,339,348-1,339,348 MRPL20, RN7SL657P
    nsv5064951mobile element insertion1nstd203human GRCh38 chr1: 1,403,973-1,403,973 , GRCh37.p13 chr1: 1,339,353-1,339,353 RN7SL657P, MRPL20
    nsv4905963copy number variation1nstd200human GRCh38 chr1: 1,403,362-1,403,949 , GRCh37.p13 chr1: 1,338,742-1,339,329 MRPL20, RN7SL657P
    nsv4782557copy number variation1nstd200human GRCh37 chr1: 1,338,891-1,339,789 , GRCh38.p12 chr1: 1,403,511-1,404,409 RN7SL657P, MRPL20
    nsv4782556copy number variation1nstd200human GRCh37 chr1: 1,338,747-1,339,327 , GRCh38.p12 chr1: 1,403,367-1,403,947 RN7SL657P, MRPL20
    nsv4782555copy number variation1nstd200human GRCh37 chr1: 1,332,300-1,338,855 , GRCh38.p12 chr1: 1,396,920-1,403,475 CCNL2, RN7SL657P, 2 more genes
    nsv4769317copy number variation1nstd102humanPathogenic GRCh37 chr1: 753,462-1,717,335 , GRCh38.p12 chr1: 818,082-1,785,896 MMP23B, DVL1, 76 more genes
    nsv4728693copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-2,033,256 , GRCh38.p12 chr1: 914,086-2,101,817 SDF4, GNB1-DT, 80 more genes
    nsv4728279copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 849,466-1,806,659 , GRCh38.p12 chr1: 914,086-1,875,220 CDK11B, DVL1, 70 more genes
    nsv4728263copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-1,976,788 , GRCh38.p12 chr1: 914,086-2,045,349 VWA1, MRPL20, 78 more genes
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