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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127383copy number variation1nstd186human GRCh37 chr22: 43,101,766-43,102,084 , GRCh38.p12 chr22: 42,705,760-42,706,078 A4GALT
    nsv6126684copy number variation1nstd186human GRCh37 chr22: 43,101,190-43,102,189 , GRCh38.p12 chr22: 42,705,184-42,706,183 A4GALT
    nsv5966307copy number variation1nstd209human GRCh38 chr22: 42,706,664-42,708,470 , GRCh37.p13 chr22: 43,102,670-43,104,476 A4GALT
    nsv5957493copy number variation1nstd209human GRCh38 chr22: 42,705,411-42,705,812 , GRCh37.p13 chr22: 43,101,417-43,101,818 A4GALT
    nsv5954521copy number variation1nstd209human GRCh38 chr22: 42,705,440-42,706,191 , GRCh37.p13 chr22: 43,101,446-43,102,197 A4GALT
    nsv5953218copy number variation1nstd209human GRCh38 chr22: 42,712,849-42,713,009 , GRCh37.p13 chr22: 43,108,855-43,109,015 A4GALT
    nsv5948527copy number variation1nstd209human GRCh38 chr22: 42,702,644-42,703,011 , GRCh37.p13 chr22: 43,098,650-43,099,017 A4GALT
    nsv5874699copy number variation1nstd209human GRCh38 chr22: 42,706,809-42,708,466 , GRCh37.p13 chr22: 43,102,815-43,104,472 A4GALT
    nsv5726824mobile element insertion1nstd211human GRCh38 chr22: 42,718,204-42,718,204 , GRCh37.p13 chr22: 43,114,210-43,114,210 A4GALT
    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
    nsv5591688copy number variation1nstd207human GRCh38 chr22: 42,705,440-42,706,191 , GRCh37.p13 chr22: 43,101,446-43,102,197 A4GALT
    nsv5584831copy number variation1nstd207human GRCh38 chr22: 42,702,644-42,703,011 , GRCh37.p13 chr22: 43,098,650-43,099,017 A4GALT
    nsv5552878copy number variation1nstd206human GRCh38 chr22: 42,705,730-42,706,107 , GRCh37.p13 chr22: 43,101,736-43,102,113 A4GALT
    nsv5552012copy number variation1nstd206human GRCh38 chr22: 42,705,184-42,706,183 , GRCh37.p13 chr22: 43,101,190-43,102,189 A4GALT
    nsv5548981copy number variation1nstd206human GRCh38 chr22: 42,702,648-42,703,012 , GRCh37.p13 chr22: 43,098,654-43,099,018 A4GALT
    nsv5547667copy number variation1nstd206human GRCh38 chr22: 42,706,282-42,707,596 , GRCh37.p13 chr22: 43,102,288-43,103,602 A4GALT
    nsv5536296copy number variation1nstd206human GRCh38 chr22: 42,705,507-42,705,943 , GRCh37.p13 chr22: 43,101,513-43,101,949 A4GALT
    nsv5535271copy number variation1nstd206human GRCh38 chr22: 42,706,664-42,708,471 , GRCh37.p13 chr22: 43,102,670-43,104,477 A4GALT
    nsv5534602copy number variation1nstd206human GRCh38 chr22: 42,702,618-42,704,843 , GRCh37.p13 chr22: 43,098,624-43,100,849 A4GALT
    nsv5391351copy number variation3nstd186human GRCh37 chr22: 43,098,654-43,099,018 , GRCh38.p12 chr22: 42,702,648-42,703,012 A4GALT
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