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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4406881copy number variation1nstd174human GRCh37 chr6: 37,339,897-37,343,468 , GRCh38.p12 chr6: 37,372,121-37,375,692 RNF8
    esv2498217copy number variation1estd197human NCBI36 chr6: 37,447,875-37,451,446 , GRCh37.p13 chr6: 37,339,897-37,343,468 , GRCh38.p12 chr6: 37,372,121-37,375,692 RNF8

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