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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112709copy number variation1nstd102humanPathogenic GRCh37 chr3: 123,000,000-129,700,000 , GRCh38.p12 chr3: 123,281,153-129,981,157 OR7E97P, MARK3P3, 160 more genes
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv5965047insertion1nstd209human GRCh38 chr3: 123,396,791-123,396,791 , GRCh37.p13 chr3: 123,115,638-123,115,638 ADCY5
    nsv5956485insertion1nstd209human GRCh38 chr3: 123,407,765-123,407,765 , GRCh37.p13 chr3: 123,126,612-123,126,612 ADCY5
    nsv5955670insertion1nstd209human GRCh38 chr3: 123,289,309-123,289,309 , GRCh37.p13 chr3: 123,008,156-123,008,156 ADCY5
    nsv5954707insertion1nstd209human GRCh38 chr3: 123,348,036-123,348,036 , GRCh37.p13 chr3: 123,066,883-123,066,883 ADCY5
    nsv5951852insertion1nstd209human GRCh38 chr3: 123,388,150-123,388,150 , GRCh37.p13 chr3: 123,106,997-123,106,997 ADCY5
    nsv5905053copy number variation1nstd209human GRCh38 chr3: 123,402,399-123,404,292 , GRCh37.p13 chr3: 123,121,246-123,123,139 ADCY5
    nsv5889078copy number variation1nstd209human GRCh38 chr3: 123,407,777-123,408,370 , GRCh37.p13 chr3: 123,126,624-123,127,217 ADCY5
    nsv5834564copy number variation1nstd209human GRCh38 chr3: 123,402,419-123,404,327 , GRCh37.p13 chr3: 123,121,266-123,123,174 ADCY5
    nsv5727806mobile element insertion2nstd211human GRCh38 chr3: 123,314,873-123,314,873 , GRCh37.p13 chr3: 123,033,720-123,033,720 ADCY5
    nsv5726268mobile element insertion2nstd211human GRCh38 chr3: 123,289,326-123,289,326 , GRCh37.p13 chr3: 123,008,173-123,008,173 ADCY5
    nsv5688362mobile element insertion1nstd211human GRCh38 chr3: 123,298,846-123,298,846 , GRCh37.p13 chr3: 123,017,693-123,017,693 ADCY5
    nsv5619917insertion1nstd207human GRCh38 chr3: 123,396,013-123,396,013 , GRCh37.p13 chr3: 123,114,860-123,114,860 ADCY5
    nsv5616691insertion1nstd207human GRCh38 chr3: 123,314,855-123,314,855 , GRCh37.p13 chr3: 123,033,702-123,033,702 ADCY5
    nsv5613773insertion1nstd207human GRCh38 chr3: 123,407,765-123,407,765 , GRCh37.p13 chr3: 123,126,612-123,126,612 ADCY5
    nsv5561323mobile element insertion1nstd206human GRCh38 chr3: 123,289,326-123,289,377 , GRCh37.p13 chr3: 123,008,173-123,008,224 ADCY5
    nsv5538088insertion1nstd206human GRCh38 chr3: 123,313,014-123,313,014 , GRCh37.p13 chr3: 123,031,861-123,031,861 ADCY5
    nsv5452030copy number variation1nstd206human GRCh38 chr3: 123,375,531-123,376,569 , GRCh37.p13 chr3: 123,094,378-123,095,416 ADCY5
    nsv5449871copy number variation1nstd206human GRCh38 chr3: 123,402,404-123,404,293 , GRCh37.p13 chr3: 123,121,251-123,123,140 ADCY5
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