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Items: 3

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    Number of Variants: 3

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5059992copy number variation1nstd102humanPathogenic GRCh37 chr7: 117,244,921-117,252,122 , GRCh38 chr7: 117,604,867-117,612,068 CFTR
    nsv4578510copy number variation1nstd102humanPathogenic GRCh37 chr7: 117,232,038-117,232,121 , GRCh38 chr7: 117,591,984-117,592,067 CFTR
    nsv3883463copy number variation1nstd102humanPathogenic GRCh37 chr7: 117,138,363-117,159,446 , GRCh38 chr7: 117,498,309-117,519,392 CFTR
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