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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4415842copy number variation1nstd174human GRCh37 chr17: 78,329,101-78,329,712 , GRCh38.p12 chr17: 80,355,301-80,355,912 RNF213, RNF213-AS1
    esv2716376copy number variation19estd201human GRCh37 chr17: 78,328,786-78,329,800 , GRCh38.p12 chr17: 80,354,986-80,356,000 RNF213-AS1, RNF213

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