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Items: 1 to 20 of 308

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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
    nsv5966926insertion1nstd209human GRCh38 chr5: 43,541,687-43,541,687 , GRCh37.p13 chr5: 43,541,789-43,541,789 PAIP1
    nsv5962961insertion1nstd209human GRCh38 chr5: 43,531,656-43,531,656 , GRCh37.p13 chr5: 43,531,758-43,531,758 PAIP1
    nsv5905642copy number variation1nstd209human GRCh38 chr5: 43,524,174-43,524,287 , GRCh37.p13 chr5: 43,524,276-43,524,389 PAIP1
    nsv5897757copy number variation1nstd209human GRCh38 chr5: 43,549,979-43,550,723 , GRCh37.p13 chr5: 43,550,081-43,550,825 PAIP1
    nsv5842995copy number variation1nstd209human GRCh38 chr5: 43,541,203-43,542,908 , GRCh37.p13 chr5: 43,541,305-43,543,010 PAIP1
    nsv5693529mobile element insertion2nstd211human GRCh38 chr5: 43,541,703-43,541,703 , GRCh37.p13 chr5: 43,541,805-43,541,805 PAIP1
    nsv5643345insertion1nstd207human GRCh38 chr5: 43,541,687-43,541,687 , GRCh37.p13 chr5: 43,541,789-43,541,789 PAIP1
    nsv5624922insertion1nstd207human GRCh38 chr5: 43,541,207-43,541,207 , GRCh37.p13 chr5: 43,541,309-43,541,309 PAIP1
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5466276copy number variation1nstd206human GRCh38 chr5: 43,549,843-43,550,781 , GRCh37.p13 chr5: 43,549,945-43,550,883 PAIP1
    nsv5460134copy number variation1nstd206human GRCh38 chr5: 43,531,379-43,532,390 , GRCh37.p13 chr5: 43,531,481-43,532,492 PAIP1
    nsv5455012copy number variation1nstd206human GRCh38 chr5: 43,524,174-43,524,288 , GRCh37.p13 chr5: 43,524,276-43,524,390 PAIP1
    nsv5402094mobile element insertion1nstd206human GRCh38 chr5: 43,541,687-43,541,687 , GRCh37.p13 chr5: 43,541,789-43,541,789 PAIP1
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5368248translocation1nstd200human GRCh38 chr5: 43,550,724-43,550,724 , GRCh38 chr5: 43,549,979-43,549,979 , GRCh37.p13 chr5: 43,550,081-43,550,081 , GRCh37.p13 chr5: 43,550,826-43,550,826 PAIP1
    nsv5330235translocation1nstd200human GRCh37 chr5: 43,550,826-43,550,826 , GRCh37 chr5: 43,550,081-43,550,081 , GRCh38.p12 chr5: 43,549,979-43,549,979 , GRCh38.p12 chr5: 43,550,724-43,550,724 PAIP1
    nsv5324591translocation1nstd204human GRCh38.p13 chr5: 43,550,724-43,550,724 , GRCh38.p13 chr5: 43,549,978-43,549,978 , GRCh37.p13 chr5: 43,550,080-43,550,080 , GRCh37.p13 chr5: 43,550,826-43,550,826 PAIP1
    nsv5234131copy number variation1nstd204human GRCh38.p13 chr5: 43,550,001-43,550,700 , GRCh37.p13 chr5: 43,550,103-43,550,802 PAIP1
    nsv5232433copy number variation1nstd204human GRCh38.p13 chr5: 43,549,936-43,551,014 , GRCh37.p13 chr5: 43,550,038-43,551,116 PAIP1
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