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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673255copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr1: 54,999,177-55,064,863 , GRCh37 chr1: 55,464,850-55,530,536 BSND, USP24, 1 more genes
    nsv3886486copy number variation1nstd102humanUncertain significance GRCh38 chr1: 55,043,823-55,044,054 , GRCh37 chr1: 55,509,496-55,509,727 PCSK9

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