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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv984636copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984635copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984634copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984633copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984632copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984631copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984630copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984629copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984628copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984627copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984626copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984623copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984620copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984618copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984617copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984616copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984615copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984614copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984613copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
    nsv984612copy number variation1nstd92human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 , ACTG1P2, 525 more genes
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