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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1077341copy number variation1nstd99human GRCh37 chr19: 34,118,299-34,122,400 , GRCh38.p12 chr19: 33,627,393-33,631,494 CHST8

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