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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381707copy number variation2nstd102humanUncertain significance GRCh37 chr9: 34,458,994-35,072,710 , GRCh38.p12 chr9: 34,458,996-35,072,713 YWHAZP6, IL11RA, 30 more genes
    nsv3871524copy number variation1nstd102humanUncertain significance GRCh37 chr9: 34,458,984-36,277,059 , GRCh38.p12 chr9: 34,458,986-36,277,062 OR2AM1P, SYF2P2, 84 more genes

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