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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114629copy number variation1nstd186human GRCh37 chr22: 42,519,569-42,536,111 , GRCh38.p12 chr22|NT_187682.1: 45,908-62,450 , CYP2D7, 4 more genes
    nsv5954144copy number variation1nstd209human GRCh38 chr22: 42,121,553-42,132,728 , GRCh37.p13 chr22: 42,518,517-42,528,735 , CYP2D6, 2 more genes
    nsv5878114copy number variation3nstd209human GRCh38 chr22: 42,128,465-42,138,065 , GRCh37.p13 chr22: 42,524,467-42,534,074 , CYP2D6, 2 more genes
    nsv5875829copy number variation3nstd209human GRCh38 chr22: 42,126,382-42,138,065 , GRCh37.p13 chr22: 42,522,384-42,534,074 , CYP2D6, 2 more genes
    nsv5874773copy number variation3nstd209human GRCh38 chr22: 42,127,325-42,130,522 , GRCh37.p13 chr22: 42,523,327-42,526,524 , CYP2D6
    nsv5673276copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,440,000-43,780,000 , GRCh38.p12 chr22: 42,043,996-43,383,994 RPL5P34, ARFGAP3, 48 more genes
    nsv5585870copy number variation1nstd207human GRCh38 chr22: 42,125,912-42,138,063 , GRCh37.p13 chr22: 42,521,917-42,534,072 , CYP2D7, 2 more genes
    nsv5415756copy number variation1nstd206human GRCh38 chr22: 42,123,564-42,140,100 , GRCh37.p13 chr22: 42,519,569-42,536,111 , CYP2D7, 4 more genes
    nsv5381149copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,333,802-51,195,728 , GRCh38.p12 chr22: 41,937,798-50,757,300 WBP2NL, RN7SKP80, 210 more genes
    nsv5381088copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,356,886-43,684,002 , GRCh38.p12 chr22: 41,960,882-43,287,996 CYP2D8P, SCUBE1, 49 more genes
    nsv5296151copy number variation1nstd204human GRCh38.p13 chr22: 42,130,201-42,135,400 , GRCh37.p13 chr22: 42,526,203-42,531,409 , LOC102723722, 1 more genes
    nsv5294686copy number variation1nstd204human GRCh38.p13 chr22: 42,130,001-42,131,400 , GRCh37.p13 chr22: 42,526,003-42,527,402 , CYP2D6
    nsv5294178copy number variation1nstd204human GRCh38.p13 chr22: 42,127,201-42,129,900 , GRCh37.p13 chr22: 42,523,203-42,525,902 , CYP2D6
    nsv5294163copy number variation1nstd204human GRCh38.p13 chr22: 41,962,701-42,147,200 , GRCh37.p13 chr22: 42,358,705-42,518,516 , SNORD13P1, 15 more genes
    nsv5290811copy number variation1nstd204human GRCh38.p13 chr22: 42,125,888-42,130,422 , GRCh37.p13 chr22: 42,521,893-42,526,424 , CYP2D6
    nsv5288022copy number variation1nstd204human GRCh38.p13 chr22: 42,122,001-42,129,800 , GRCh37.p13 chr22: 42,518,517-42,525,802 , 2 more genes
    nsv5286067copy number variation1nstd204human GRCh37.p13 chr22: 42,520,906-42,543,489 , GRCh38.p13 chr22: 42,124,901-42,147,500 , CYP2D7, 4 more genes
    nsv5285689copy number variation1nstd204human GRCh37.p13 chr22: 42,519,305-42,539,901 , GRCh38.p13 chr22: 42,123,301-42,143,900 , CYP2D7, 5 more genes
    nsv5285395copy number variation1nstd204human GRCh38.p13 chr22: 42,123,501-42,127,600 , GRCh37.p13 chr22: 42,519,506-42,523,602 , CYP2D6, 1 more genes
    nsv5284246copy number variation1nstd204human GRCh37.p13 chr22: 42,519,005-42,533,709 , GRCh38.p13 chr22: 42,123,001-42,137,700 , CYP2D7, 4 more genes
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