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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4449617copy number variation1nstd45humanPathogenic GRCh38.p12 chr1: 244,048,939-244,057,476 , GRCh37 chr1: 244,212,241-244,220,778 ZBTB18

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