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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4425631copy number variation1nstd174human GRCh37 chr10: 132,908,468-132,914,909 , GRCh38.p12 chr10: 131,110,205-131,116,646 TCERG1L
    esv3624951copy number variation1022estd214human GRCh37 chr10: 132,909,082-132,912,781 , GRCh38.p12 chr10: 131,110,819-131,114,518 TCERG1L

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