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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4402530copy number variation1nstd174human GRCh37 chr3: 1,044,150-1,046,237 , GRCh38.p12 chr3: 1,002,466-1,004,553 CNTN6
    esv3594940copy number variation23estd214human GRCh37 chr3: 1,044,148-1,046,222 , GRCh38.p12 chr3: 1,002,464-1,004,538 CNTN6

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