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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4681186copy number variation2nstd102humanUncertain significance GRCh37 chr3: 14,166,684-14,183,305 , GRCh38.p12 chr3: 14,125,184-14,141,805 TMEM43, CHCHD4
    nsv3883133copy number variation1nstd102humanUncertain significance GRCh37 chr3: 14,166,440-14,185,180 , GRCh38 chr3: 14,124,940-14,143,680 TMEM43, XPC, 1 more genes

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