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Items: 1 to 20 of 1804

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139705copy number variation1nstd232human GRCh37.p13 chr3: 71,484,425-71,484,528 , GRCh38.p12 chr3: 71,435,274-71,435,377 FOXP1
    nsv7098863copy number variation1nstd102humannot provided GRCh37 chr3: 71,021,211-71,181,046 , GRCh38.p12 chr3: 70,972,060-71,131,895 FOXP1
    nsv7097214copy number variation1nstd102humanPathogenic GRCh37 chr3: 71,247,333-71,480,567 , GRCh38.p12 chr3: 71,198,182-71,431,416 FOXP1, FOXP1-AS1
    nsv7048031inversion1nstd229human GRCh38 chr3: 71,463,895-71,464,023 , GRCh37.p13 chr3: 71,513,046-71,513,174 FOXP1
    nsv7044441inversion1nstd229human GRCh38 chr3: 71,500,392-71,504,669 , GRCh37.p13 chr3: 71,549,543-71,553,820 FOXP1
    nsv6716983copy number variation1nstd229human GRCh38 chr3: 70,969,708-70,969,789 , GRCh37.p13 chr3: 71,018,859-71,018,940 FOXP1
    nsv6716441copy number variation1nstd229human GRCh38 chr3: 71,032,787-71,035,872 , GRCh37.p13 chr3: 71,081,938-71,085,023 FOXP1
    nsv6716167copy number variation1nstd229human GRCh38 chr3: 71,135,378-71,135,507 , GRCh37.p13 chr3: 71,184,529-71,184,658 FOXP1
    nsv6716042copy number variation1nstd229human GRCh38 chr3: 71,317,906-71,318,648 , GRCh37.p13 chr3: 71,367,057-71,367,799 FOXP1
    nsv6715402copy number variation1nstd229human GRCh38 chr3: 71,487,426-71,493,138 , GRCh37.p13 chr3: 71,536,577-71,542,289 FOXP1
    nsv6714557copy number variation1nstd229human GRCh38 chr3: 71,473,475-71,473,581 , GRCh37.p13 chr3: 71,522,626-71,522,732 FOXP1
    nsv6714109copy number variation1nstd229human GRCh38 chr3: 71,333,654-71,335,601 , GRCh37.p13 chr3: 71,382,805-71,384,752 FOXP1
    nsv6714018copy number variation1nstd229human GRCh38 chr3: 71,132,048-71,142,161 , GRCh37.p13 chr3: 71,181,199-71,191,312 FOXP1
    nsv6713733copy number variation1nstd229human GRCh38 chr3: 71,351,401-71,354,500 , GRCh37.p13 chr3: 71,400,552-71,403,651 FOXP1
    nsv6713618copy number variation1nstd229human GRCh38 chr3: 71,441,118-71,442,251 , GRCh37.p13 chr3: 71,490,269-71,491,402 FOXP1
    nsv6713535copy number variation1nstd229human GRCh38 chr3: 71,376,262-71,379,542 , GRCh37.p13 chr3: 71,425,413-71,428,693 FOXP1
    nsv6713354copy number variation1nstd229human GRCh38 chr3: 71,551,365-71,565,022 , GRCh37.p13 chr3: 71,600,516-71,614,173 FOXP1
    nsv6713258copy number variation1nstd229human GRCh38 chr3: 71,448,117-71,451,539 , GRCh37.p13 chr3: 71,497,268-71,500,690 FOXP1
    nsv6713217copy number variation1nstd229human GRCh38 chr3: 71,469,828-71,476,871 , GRCh37.p13 chr3: 71,518,979-71,526,022 FOXP1
    nsv6713051copy number variation1nstd229human GRCh38 chr3: 71,540,401-71,545,400 , GRCh37.p13 chr3: 71,589,552-71,594,551 FOXP1, MIR1284
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