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Items: 5

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    Number of Variants: 5

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6626716copy number variation32nstd224human GRCh37 chr20: 58,440,438-58,502,456 , GRCh38.p12 chr20: 59,865,383-59,927,401 SYCP2
    nsv6628914copy number variation179nstd224human GRCh37 chr3: 173,259,356-173,289,281 , GRCh38.p12 chr3: 173,541,566-173,571,491 NLGN1
    nsv6624844copy number variation645nstd224human GRCh37 chr19: 20,630,360-20,715,228 , GRCh38.p12 chr19: 20,447,554-20,532,422 ZNF737, LOC105372316, 1 more genes
    nsv6624765copy number variation10nstd224human GRCh37 chr19: 43,654,209-43,708,179 , GRCh38.p12 chr19: 43,150,057-43,204,027 PSG5, PSG4, 1 more genes
    nsv6625917copy number variation63nstd224human GRCh37 chr1: 17,216,331-17,266,464 , GRCh38.p12 chr1: 16,889,836-16,939,969 CROCC, LOC105376805, 3 more genes
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