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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4396759copy number variation1nstd174human GRCh37 chr3: 191,064,001-191,073,706 , GRCh38.p12 chr3: 191,346,212-191,355,917 CCDC50
    esv3599104copy number variation622estd214human GRCh37 chr3: 191,064,294-191,072,037 , GRCh38.p12 chr3: 191,346,505-191,354,248 CCDC50

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