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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138228insertion1nstd232human GRCh37.p13 chr22: 42,140,491-42,140,491 , GRCh38.p12 chr22: 41,744,487-41,744,487 MEI1
    nsv7096308copy number variation1nstd102humanUncertain significance GRCh37 chr22: 35,776,672-42,486,826 , GRCh38.p12 chr22: 35,380,679-42,090,822 CDC42EP1, SREBF2, 231 more genes
    nsv7072908inversion1nstd229human GRCh38 chr22: 41,741,990-41,742,683 , GRCh37.p13 chr22: 42,137,994-42,138,687 MEI1
    nsv7072405inversion1nstd229human GRCh38 chr22: 41,714,365-41,714,407 , GRCh37.p13 chr22: 42,110,369-42,110,411 MEI1
    nsv7072360inversion1nstd229human GRCh38 chr22: 41,725,628-41,725,692 , GRCh37.p13 chr22: 42,121,632-42,121,696 MEI1
    nsv7069304inversion1nstd229human GRCh38 chr22: 41,294,727-42,750,704 , GRCh37.p13 chr22: 41,690,731-43,146,710 SERHL2, CSDC2, 63 more genes
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7058666inversion1nstd229human GRCh38 chr22: 39,066,437-42,707,681 , GRCh37.p13 chr22: 39,462,442-43,103,687 LOC101927344, ATF4, 128 more genes
    nsv7036552copy number variation1nstd229human GRCh38 chr22: 41,712,735-41,727,878 , GRCh37.p13 chr22: 42,108,739-42,123,882 RNU6ATAC22P, MEI1
    nsv7036106copy number variation1nstd229human GRCh38 chr22: 41,726,101-41,728,400 , GRCh37.p13 chr22: 42,122,105-42,124,404 MEI1
    nsv7035933copy number variation1nstd229human GRCh38 chr22: 41,765,147-41,769,750 , GRCh37.p13 chr22: 42,161,151-42,165,754 MEI1
    nsv7035714copy number variation1nstd229human GRCh38 chr22: 41,692,369-41,719,693 , GRCh37.p13 chr22: 42,088,373-42,115,697 HMGN2P10, C22orf46P, 1 more genes
    nsv7033300copy number variation1nstd229human GRCh38 chr22: 41,693,489-41,704,383 , GRCh37.p13 chr22: 42,089,493-42,100,387 C22orf46P, MEI1
    nsv7031860copy number variation1nstd229human GRCh38 chr22: 41,721,116-41,734,591 , GRCh37.p13 chr22: 42,117,120-42,130,595 RNU6ATAC22P, MEI1
    nsv7030049copy number variation1nstd229human GRCh38 chr22: 41,793,289-41,797,248 , GRCh37.p13 chr22: 42,189,293-42,193,252 MEI1
    nsv7029168copy number variation1nstd229human GRCh38 chr22: 41,712,869-41,714,427 , GRCh37.p13 chr22: 42,108,873-42,110,431 MEI1
    nsv7027741copy number variation1nstd229human GRCh38 chr22: 39,432,386-49,047,389 , GRCh37.p13 chr22: 39,828,391-49,443,201 LOC105373064, ACO2, 233 more genes
    nsv7027042copy number variation1nstd229human GRCh38 chr22: 41,706,511-41,712,841 , GRCh37.p13 chr22: 42,102,515-42,108,845 MEI1, HMGN2P10
    nsv7025575copy number variation1nstd229human GRCh38 chr22: 41,781,601-41,831,200 , GRCh37.p13 chr22: 42,177,605-42,227,204 SREBF2-AS1, CCDC134, 2 more genes
    nsv7024893copy number variation1nstd229human GRCh38 chr22: 41,739,188-41,742,752 , GRCh37.p13 chr22: 42,135,192-42,138,756 MEI1
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