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Items: 1 to 20 of 505

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966652insertion1nstd209human GRCh38 chr9: 6,469,705-6,469,705 , GRCh37.p13 chr9: 6,469,705-6,469,705 UHRF2
    nsv5921645copy number variation1nstd209human GRCh38 chr9: 6,482,700-6,484,896 , GRCh37.p13 chr9: 6,482,700-6,484,896 UHRF2
    nsv5912823copy number variation1nstd209human GRCh38 chr9: 6,478,573-6,478,779 , GRCh37.p13 chr9: 6,478,573-6,478,779 UHRF2
    nsv5859731copy number variation1nstd209human GRCh38 chr9: 6,482,190-6,484,239 , GRCh37.p13 chr9: 6,482,190-6,484,239 UHRF2
    nsv5849418copy number variation1nstd209human GRCh38 chr9: 6,482,890-6,484,089 , GRCh37.p13 chr9: 6,482,890-6,484,089 UHRF2
    nsv5704878mobile element insertion1nstd211human GRCh38 chr9: 6,445,151-6,445,151 , GRCh37.p13 chr9: 6,445,151-6,445,151 UHRF2
    nsv5695069mobile element insertion1nstd211human GRCh38 chr9: 6,485,828-6,485,828 , GRCh37.p13 chr9: 6,485,828-6,485,828 UHRF2
    nsv5694938mobile element insertion2nstd211human GRCh38 chr9: 6,424,630-6,424,630 , GRCh37.p13 chr9: 6,424,630-6,424,630 UHRF2
    nsv5636776insertion1nstd207human GRCh38 chr9: 6,444,380-6,444,380 , GRCh37.p13 chr9: 6,444,380-6,444,380 UHRF2
    nsv5627546insertion1nstd207human GRCh38 chr9: 6,486,604-6,486,604 , GRCh37.p13 chr9: 6,486,604-6,486,604 UHRF2
    nsv5543462insertion1nstd206human GRCh38 chr9: 6,433,020-6,433,054 , GRCh37.p13 chr9: 6,433,020-6,433,054 UHRF2
    nsv5485377copy number variation1nstd206human GRCh38 chr9: 6,487,570-6,521,838 , GRCh37.p13 chr9: 6,487,570-6,521,838 UHRF2
    nsv5482146copy number variation1nstd206human GRCh38 chr9: 6,434,682-6,435,907 , GRCh37.p13 chr9: 6,434,682-6,435,907 UHRF2
    nsv5404259mobile element insertion1nstd206human GRCh38 chr9: 6,424,630-6,424,645 , GRCh37.p13 chr9: 6,424,630-6,424,645 UHRF2
    nsv5381785copy number variation1nstd102humanPathogenic GRCh37 chr9: 2,854,435-6,937,677 , GRCh38.p12 chr9: 2,854,435-6,937,677 GLIS3-AS1, RFX3-DT, 70 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 ACTG1P14, DMAC1, 191 more genes
    nsv5196150mobile element insertion1nstd203human GRCh38 chr9: 6,464,486-6,464,499 , GRCh37.p13 chr9: 6,464,486-6,464,499 UHRF2
    nsv5113602mobile element insertion1nstd203human GRCh38 chr9: 6,502,790-6,502,805 , GRCh37.p13 chr9: 6,502,790-6,502,805 UHRF2
    nsv5110819mobile element insertion1nstd203human GRCh38 chr9: 6,502,794-6,502,805 , GRCh37.p13 chr9: 6,502,794-6,502,805 UHRF2
    nsv5100389mobile element insertion1nstd203human GRCh38 chr9: 6,502,793-6,502,805 , GRCh37.p13 chr9: 6,502,793-6,502,805 UHRF2
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