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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv954902copy number variation1nstd73human GRCh37 chr1: 21,926,201-21,981,000 , GRCh38.p12 chr1: 21,599,708-21,654,507 RAP1GAP

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