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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1071497copy number variation1nstd99human GRCh37 chr19: 3,365,999-3,366,600 , GRCh38.p12 chr19: 3,366,001-3,366,602 NFIC

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