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Items: 1 to 20 of 442

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5905391copy number variation1nstd209human GRCh38 chr5: 39,272,001-39,272,058 , GRCh37.p13 chr5: 39,272,103-39,272,160 FYB1
    nsv5905356copy number variation1nstd209human GRCh38 chr5: 39,262,225-39,263,104 , GRCh37.p13 chr5: 39,262,327-39,263,206 FYB1
    nsv5905296copy number variation1nstd209human GRCh38 chr5: 39,213,678-39,214,160 , GRCh37.p13 chr5: 39,213,780-39,214,262 FYB1
    nsv5898511copy number variation1nstd209human GRCh38 chr5: 39,179,581-39,183,057 , GRCh37.p13 chr5: 39,179,683-39,183,159 FYB1
    nsv5842719copy number variation1nstd209human GRCh38 chr5: 39,177,979-39,182,876 , GRCh37.p13 chr5: 39,178,081-39,182,978 FYB1
    nsv5716922mobile element insertion1nstd211human GRCh38 chr5: 39,245,181-39,245,181 , GRCh37.p13 chr5: 39,245,283-39,245,283 FYB1
    nsv5684902mobile element insertion2nstd211human GRCh38 chr5: 39,231,754-39,231,754 , GRCh37.p13 chr5: 39,231,856-39,231,856 FYB1
    nsv5678825mobile element insertion1nstd211human GRCh38 chr5: 39,256,882-39,256,882 , GRCh37.p13 chr5: 39,256,984-39,256,984 FYB1
    nsv5676936mobile element insertion1nstd211human GRCh38 chr5: 39,240,510-39,240,510 , GRCh37.p13 chr5: 39,240,612-39,240,612 FYB1
    nsv5630013insertion1nstd207human GRCh38 chr5: 39,231,742-39,231,742 , GRCh37.p13 chr5: 39,231,844-39,231,844 FYB1
    nsv5626528insertion1nstd207human GRCh38 chr5: 39,253,540-39,253,540 , GRCh37.p13 chr5: 39,253,642-39,253,642 FYB1
    nsv5583137copy number variation1nstd207human GRCh38 chr5: 39,272,001-39,272,058 , GRCh37.p13 chr5: 39,272,103-39,272,160 FYB1
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5467793copy number variation1nstd206human GRCh38 chr5: 39,264,716-39,264,829 , GRCh37.p13 chr5: 39,264,818-39,264,931 FYB1
    nsv5467710copy number variation1nstd206human GRCh38 chr5: 39,213,678-39,214,161 , GRCh37.p13 chr5: 39,213,780-39,214,263 FYB1
    nsv5462120copy number variation1nstd206human GRCh38 chr5: 39,272,001-39,272,059 , GRCh37.p13 chr5: 39,272,103-39,272,161 FYB1
    nsv5459411copy number variation1nstd206human GRCh38 chr5: 39,198,580-39,198,667 , GRCh37.p13 chr5: 39,198,682-39,198,769 FYB1
    nsv5459139copy number variation1nstd206human GRCh38 chr5: 39,179,561-39,183,098 , GRCh37.p13 chr5: 39,179,663-39,183,200 FYB1
    nsv5454427copy number variation1nstd206human GRCh38 chr5: 39,262,225-39,263,109 , GRCh37.p13 chr5: 39,262,327-39,263,211 FYB1
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