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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3871139copy number variation3nstd102humanPathogenic GRCh37 chr19: 13,054,565-13,054,616 , GRCh38 chr19: 12,943,751-12,943,802 CALR
    nsv1398076copy number variation4nstd102humanLikely pathogenic GRCh37 chr14: 96,163,103-96,857,129 , GRCh38 chr14: 95,696,766-96,390,792 BDKRB1, BDKRB2, 10 more genes

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