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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137865copy number variation2nstd102humanrisk factor NCBI35 chr22: 27,408,285-27,462,376 , GRCh37.p13 chr22: 29,083,731-29,137,822 , GRCh38.p12 chr22: 28,687,743-28,741,834 CHEK2, HSCB

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