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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4683415copy number variation1nstd102humanUncertain significance GRCh37 chr13: 20,716,100-21,398,980 , GRCh38.p12 chr13: 20,141,961-20,824,841 GJB6, EEF1AKMT1, 14 more genes
    nsv3889090copy number variation1nstd102humanUncertain significance GRCh38 chr13: 20,141,961-20,143,308 , GRCh37 chr13: 20,716,100-20,717,447 GJA3

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