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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146518copy number variation1nstd232human GRCh37.p13 chr5: 122,723,707-122,723,762 , GRCh38.p12 chr5: 123,388,013-123,388,068 CEP120
    nsv7051275inversion1nstd229human GRCh38 chr5: 123,400,567-123,400,604 , GRCh37.p13 chr5: 122,736,261-122,736,298 CEP120, KRT8P33
    nsv7047334inversion1nstd229human GRCh38 chr5: 119,494,072-128,765,801 , GRCh37.p13 chr5: 118,829,767-128,101,494 RPL18P3, KRT18P16, 98 more genes
    nsv7044021inversion1nstd229human GRCh38 chr5: 123,369,658-123,369,768 , GRCh37.p13 chr5: 122,705,352-122,705,462 CEP120
    nsv7039392inversion1nstd229human GRCh38 chr5: 120,520,478-123,368,624 , GRCh37.p13 chr5: 119,856,173-122,704,318 PPIC-AS1, LOC101927357, 34 more genes
    nsv6777725copy number variation1nstd229human GRCh38 chr5: 123,275,548-123,574,881 , GRCh37.p13 chr5: 122,611,242-122,910,575 HMGB3P17, KRT8P33, 2 more genes
    nsv6777068copy number variation1nstd229human GRCh38 chr5: 123,350,701-123,350,804 , GRCh37.p13 chr5: 122,686,395-122,686,498 CEP120
    nsv6776575copy number variation1nstd229human GRCh38 chr5: 123,390,225-123,403,134 , GRCh37.p13 chr5: 122,725,919-122,738,828 KRT8P33, CEP120
    nsv6775974copy number variation1nstd229human GRCh38 chr5: 123,359,201-123,375,800 , GRCh37.p13 chr5: 122,694,895-122,711,494 CEP120
    nsv6774802copy number variation1nstd229human GRCh38 chr5: 123,355,946-123,361,827 , GRCh37.p13 chr5: 122,691,640-122,697,521 CEP120
    nsv6773841copy number variation1nstd229human GRCh38 chr5: 123,413,446-123,419,393 , GRCh37.p13 chr5: 122,749,140-122,755,087 CEP120
    nsv6767063copy number variation1nstd229human GRCh38 chr5: 123,361,191-123,361,282 , GRCh37.p13 chr5: 122,696,885-122,696,976 CEP120
    nsv6765658copy number variation1nstd229human GRCh38 chr5: 123,388,013-123,388,069 , GRCh37.p13 chr5: 122,723,707-122,723,763 CEP120
    nsv6764322copy number variation1nstd229human GRCh38 chr5: 123,322,839-124,149,356 , GRCh37.p13 chr5: 122,658,533-123,485,049 KRT8P33, LINC01170, 5 more genes
    nsv6763250copy number variation1nstd229human GRCh38 chr5: 123,385,201-123,470,400 , GRCh37.p13 chr5: 122,720,895-122,806,094 CEP120, KRT8P33, 1 more genes
    nsv6763080copy number variation1nstd229human GRCh38 chr5: 123,414,692-123,419,923 , GRCh37.p13 chr5: 122,750,386-122,755,617 CEP120
    nsv6761888copy number variation1nstd229human GRCh38 chr5: 123,404,257-123,404,478 , GRCh37.p13 chr5: 122,739,951-122,740,172 CEP120
    nsv6760548copy number variation1nstd229human GRCh38 chr5: 123,420,326-123,441,203 , GRCh37.p13 chr5: 122,756,020-122,776,897 CEP120
    nsv6637111copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,557,391-128,106,299 , GRCh38.p12 chr5: 113,221,694-128,770,606 SLC12A2, CCDC192, 180 more genes
    nsv6636228copy number variation1nstd102humanUncertain significance GRCh37 chr5: 122,610,315-122,912,616 , GRCh38.p12 chr5: 123,274,621-123,576,922 KRT8P33, HMGB3P17, 2 more genes
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