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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3604874copy number variation1estd214human GRCh37 chr5: 42,628,085-42,758,107 , GRCh38.p12 chr5: 42,627,983-42,758,005 GHR, CCDC152
    nsv4400772copy number variation1nstd174human GRCh37 chr5: 42,610,090-42,844,191 , GRCh38.p12 chr5: 42,609,988-42,844,089 GHR, SELENOP, 1 more genes

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