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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4685584copy number variation1nstd102humanPathogenic GRCh37 chrX: 100,601,463-100,603,745 , GRCh38.p12 chrX: 101,346,475-101,348,757 BTK, TIMM8A
    nsv997091copy number variation1nstd45humanPathogenic GRCh37 chrX: 100,600,644-100,603,957 , GRCh38.p12 chrX: 101,345,656-101,348,969 BTK, TIMM8A

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