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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144930copy number variation1nstd232human GRCh37.p13 chr1: 100,148,590-100,148,643 , GRCh38.p12 chr1: 99,683,034-99,683,087 PALMD
    nsv7140706copy number variation1nstd232human GRCh37.p13 chr1: 100,148,594-100,148,643 , GRCh38.p12 chr1: 99,683,038-99,683,087 PALMD
    nsv7099219copy number variation1nstd231human GRCh38.p12 chr1: 99,594,616-101,416,026 , GRCh37 chr1: 100,060,172-101,881,582 AGL, DBT, 38 more genes
    nsv6658080copy number variation1nstd229human GRCh38 chr1: 99,685,762-99,766,762 , GRCh37.p13 chr1: 100,151,318-100,232,318 HMGB3P10, PALMD, 1 more genes
    nsv6658079copy number variation1nstd229human GRCh38 chr1: 99,661,162-99,731,008 , GRCh37.p13 chr1: 100,126,718-100,196,564 FRRS1, PALMD, 1 more genes
    nsv6657978copy number variation1nstd229human GRCh38 chr1: 99,654,003-99,704,110 , GRCh37.p13 chr1: 100,119,559-100,169,666 HMGB3P10, FRRS1, 1 more genes
    nsv6657977copy number variation1nstd229human GRCh38 chr1: 99,642,179-100,077,061 , GRCh37.p13 chr1: 100,107,735-100,542,617 MFSD14A, SLC35A3, 8 more genes
    nsv6657975copy number variation1nstd229human GRCh38 chr1: 99,498,947-100,487,486 , GRCh37.p13 chr1: 99,964,503-100,953,042 CDC14A, AGL, 21 more genes
    nsv6657894copy number variation1nstd229human GRCh38 chr1: 99,356,330-99,995,147 , GRCh37.p13 chr1: 99,821,886-100,460,703 LOC107985093, LINC01708, 8 more genes
    nsv6657521copy number variation1nstd229human GRCh38 chr1: 99,682,330-99,949,365 , GRCh37.p13 chr1: 100,147,886-100,414,921 PALMD, FRRS1, 4 more genes
    nsv6657520copy number variation1nstd229human GRCh38 chr1: 99,656,192-99,703,539 , GRCh37.p13 chr1: 100,121,748-100,169,095 HMGB3P10, PALMD, 1 more genes
    nsv6333280copy number variation1nstd223human GRCh38 chr1: 99,662,801-99,663,140 , GRCh37.p13 chr1: 100,128,357-100,128,696 PALMD
    nsv6332598copy number variation1nstd223human GRCh38 chr1: 99,642,179-100,077,059 , GRCh37.p13 chr1: 100,107,735-100,542,615 HMGB3P10, RNU6-750P, 8 more genes
    nsv6330843copy number variation1nstd223human GRCh38 chr1: 99,654,201-99,655,400 , GRCh37.p13 chr1: 100,119,757-100,120,956 PALMD
    nsv6329342copy number variation1nstd223human GRCh38 chr1: 99,480,115-99,844,212 , GRCh37.p13 chr1: 99,945,671-100,309,768 PALMD, FRRS1, 4 more genes
    nsv6329021copy number variation1nstd223human GRCh38 chr1: 99,682,330-99,949,365 , GRCh37.p13 chr1: 100,147,886-100,414,921 HMGB3P10, RNU4-75P, 4 more genes
    nsv6327756copy number variation1nstd223human GRCh38 chr1: 99,657,105-99,657,805 , GRCh37.p13 chr1: 100,122,661-100,123,361 PALMD
    nsv6321913copy number variation1nstd223human GRCh38 chr1: 99,664,701-99,665,900 , GRCh37.p13 chr1: 100,130,257-100,131,456 PALMD
    nsv6319953copy number variation1nstd223human GRCh38 chr1: 99,654,003-99,704,110 , GRCh37.p13 chr1: 100,119,559-100,169,666 HMGB3P10, FRRS1, 1 more genes
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 LINC01307, FTLP17, 320 more genes
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