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Items: 4

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    Number of Variants: 4

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5674329insertion1nstd102humanPathogenic GRCh37 chr9: 111,903,713-111,903,713 , GRCh38 chr9: 109,141,433-109,141,433 FRRS1L
    nsv5381738copy number variation1nstd102humanUncertain significance GRCh37 chr9: 111,640,893-111,929,571 , GRCh38.p12 chr9: 108,878,613-109,167,291 LOC105376216, ELP1, 6 more genes
    nsv4683934copy number variation1nstd102humanPathogenic GRCh37 chr9: 111,909,311-111,909,489 , GRCh38.p12 chr9: 109,147,031-109,147,209 FRRS1L
    nsv4681925copy number variation1nstd102humanUncertain significance GRCh37 chr9: 111,899,715-111,929,591 , GRCh38.p12 chr9: 109,137,435-109,167,311 FRRS1L
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