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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137771copy number variation1nstd102humanBenign GRCh37 chr17: 71,188,970-71,189,037 , GRCh38 chr17: 73,192,831-73,192,898 COG1
    nsv6137747copy number variation1nstd102humanBenign GRCh37 chr17: 71,188,996-71,189,076 , GRCh38 chr17: 73,192,857-73,192,937 COG1
    nsv6124578copy number variation1nstd186human GRCh37 chr17: 71,189,952-71,190,629 , GRCh38.p12 chr17: 73,193,813-73,194,490 COG1
    nsv5937071copy number variation1nstd209human GRCh38 chr17: 73,194,157-73,194,464 , GRCh37.p13 chr17: 71,190,296-71,190,603 COG1
    nsv5702273mobile element insertion1nstd211human GRCh38 chr17: 73,202,941-73,202,941 , GRCh37.p13 chr17: 71,199,080-71,199,080 COG1
    nsv5585590copy number variation1nstd207human GRCh38 chr17: 73,192,838-73,192,893 , GRCh37.p13 chr17: 71,188,977-71,189,032 COG1
    nsv5584942copy number variation1nstd207human GRCh38 chr17: 73,194,168-73,194,458 , GRCh37.p13 chr17: 71,190,307-71,190,597 COG1
    nsv5521549copy number variation1nstd206human GRCh38 chr17: 73,192,833-73,192,930 , GRCh37.p13 chr17: 71,188,972-71,189,069 COG1
    nsv5516286copy number variation1nstd206human GRCh38 chr17: 73,193,813-73,194,490 , GRCh37.p13 chr17: 71,189,952-71,190,629 COG1
    nsv5430626mobile element insertion1nstd206human GRCh38 chr17: 73,202,941-73,202,992 , GRCh37.p13 chr17: 71,199,080-71,199,131 COG1
    nsv5385328mobile element deletion1nstd186human GRCh37 chr17: 71,190,298-71,190,622 , GRCh38.p12 chr17: 73,194,159-73,194,483 COG1
    nsv5381182copy number variation1nstd102humanUncertain significance GRCh37 chr17: 71,189,189-71,189,543 , GRCh38.p12 chr17: 73,193,050-73,193,404 COG1
    nsv5375005translocation1nstd200human GRCh38 chr17: 73,200,731-73,200,731 , GRCh38 chr17: 73,195,795-73,195,795 , GRCh37.p13 chr17: 71,196,870-71,196,870 , GRCh37.p13 chr17: 71,191,934-71,191,934 COG1
    nsv5375004translocation1nstd200human GRCh38 chr17: 73,192,833-73,192,833 , GRCh38 chr17: 73,192,930-73,192,930 , GRCh37.p13 chr17: 71,188,972-71,188,972 , GRCh37.p13 chr17: 71,189,069-71,189,069 COG1
    nsv5343830translocation1nstd200human GRCh37 chr17: 71,191,934-71,191,934 , GRCh37 chr17: 71,196,870-71,196,870 , GRCh38.p12 chr17: 73,200,731-73,200,731 , GRCh38.p12 chr17: 73,195,795-73,195,795 COG1
    nsv5339721translocation1nstd200human GRCh37 chr17: 71,189,069-71,189,069 , GRCh37 chr17: 71,188,972-71,188,972 , GRCh38.p12 chr17: 73,192,930-73,192,930 , GRCh38.p12 chr17: 73,192,833-73,192,833 COG1
    nsv5322529translocation1nstd204human GRCh38.p13 chr17: 73,192,833-73,192,833 , GRCh38.p13 chr17: 73,192,930-73,192,930 , GRCh37.p13 chr17: 71,188,972-71,188,972 , GRCh37.p13 chr17: 71,189,069-71,189,069 COG1
    nsv5202845mobile element deletion1nstd204human GRCh38.p13 chr17: 73,194,118-73,194,684 , GRCh37.p13 chr17: 71,190,257-71,190,823 COG1
    nsv5140496mobile element insertion1nstd203human GRCh38 chr17: 73,202,930-73,202,941 , GRCh37.p13 chr17: 71,199,069-71,199,080 COG1
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
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