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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4684167copy number variation2nstd102humanPathogenic, protective GRCh37 chr2: 127,451,437-127,451,520 , GRCh38 chr2: 126,693,861-126,693,944 GYPC
    nsv1398576copy number variation1nstd102humanprotective GRCh37 chrX: 77,190,006-77,231,471 , GRCh38.p12 chrX: 77,934,509-77,975,975 PGAM4, ATP7A, 1 more genes

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