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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3595011copy number variation2estd214human GRCh37 chr3: 2,156,399-2,158,317 , GRCh38.p12 chr3: 2,114,715-2,116,633 CNTN4-AS2, CNTN4

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