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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6315588copy number variation1nstd222human GRCh37.p13 chr16: 85,986,306-86,727,693 , GRCh38 chr16: 85,952,700-86,694,087 FOXF1, FOXL1, 13 more genes

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