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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5380707copy number variation1nstd208human GRCh38.p12 chr22: 18,339,130-21,111,111 , GRCh37 chr22: 18,912,300-21,465,400 ARVCF, COMT, 127 more genes
    nsv5380708copy number variation1nstd208human GRCh38.p12 chr22: 18,339,130-21,105,710 , GRCh37 chr22: 18,910,000-21,459,999 ARVCF, COMT, 126 more genes

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