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Items: 6

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    Number of Variants: 6

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148236copy number variation1nstd102humanPathogenic GRCh38 chr16: 28,486,250-28,486,550 , GRCh37.p13 chr16: 28,497,571-28,497,871 CLN3
    nsv4685730copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,497,668-28,497,972 , GRCh38.p12 chr16: 28,486,347-28,486,651 CLN3
    nsv4675801copy number variation2nstd102humanPathogenic GRCh37 chr16: 28,497,668-28,497,971 , GRCh38.p12 chr16: 28,486,347-28,486,650 CLN3
    nsv4454057copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,497,280-28,498,401 , GRCh38 chr16: 28,485,959-28,487,080 CLN3
    nsv4450844copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,491,981-28,494,795 , GRCh38 chr16: 28,480,660-28,483,474 CLN3
    nsv3873873copy number variation3nstd102humanPathogenic GRCh38 chr16: 28,485,965-28,486,930 , GRCh37 chr16: 28,497,286-28,498,251 CLN3
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