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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1160537copy number variation1nstd111human GRCh37 chr1: 26,297,033-26,318,832 , GRCh38.p12 chr1: 25,970,542-25,992,341 PAFAH2

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