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Items: 1 to 20 of 247

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7044478inversion1nstd229human GRCh38 chr3: 140,992,844-142,136,153 , GRCh37.p13 chr3: 140,711,686-141,854,995 KRT18P35, SPSB4, 16 more genes
    nsv6737668copy number variation1nstd229human GRCh38 chr3: 141,100,445-141,102,963 , GRCh37.p13 chr3: 140,819,287-140,821,805 SPSB4
    nsv6736931copy number variation1nstd229human GRCh38 chr3: 141,137,997-141,260,842 , GRCh37.p13 chr3: 140,856,839-140,979,684 RPL31P21, SPSB4, 1 more genes
    nsv6733955copy number variation1nstd229human GRCh38 chr3: 141,066,892-141,190,299 , GRCh37.p13 chr3: 140,785,734-140,909,141 SPSB4
    nsv6733851copy number variation1nstd229human GRCh38 chr3: 141,127,515-141,253,755 , GRCh37.p13 chr3: 140,846,357-140,972,597 PXYLP1, SPSB4
    nsv6733119copy number variation1nstd229human GRCh38 chr3: 141,139,020-141,141,820 , GRCh37.p13 chr3: 140,857,862-140,860,662 SPSB4
    nsv6732692copy number variation1nstd229human GRCh38 chr3: 140,859,267-141,179,075 , GRCh37.p13 chr3: 140,578,109-140,897,917 SLC25A36, RPL23AP41, 1 more genes
    nsv6731718copy number variation1nstd229human GRCh38 chr3: 140,970,345-141,440,016 , GRCh37.p13 chr3: 140,689,187-141,158,858 SPSB4, PHF5AP7, 4 more genes
    nsv6730342copy number variation1nstd229human GRCh38 chr3: 141,131,901-141,144,400 , GRCh37.p13 chr3: 140,850,743-140,863,242 SPSB4
    nsv6729234copy number variation1nstd229human GRCh38 chr3: 141,146,401-141,222,800 , GRCh37.p13 chr3: 140,865,243-140,941,642 SPSB4
    nsv6728892copy number variation1nstd229human GRCh38 chr3: 141,106,250-141,112,738 , GRCh37.p13 chr3: 140,825,092-140,831,580 SPSB4
    nsv6728568copy number variation1nstd229human GRCh38 chr3: 141,056,779-141,057,161 , GRCh37.p13 chr3: 140,775,621-140,776,003 SPSB4
    nsv6728018copy number variation1nstd229human GRCh38 chr3: 141,129,032-141,134,068 , GRCh37.p13 chr3: 140,847,874-140,852,910 SPSB4
    nsv6726226copy number variation1nstd229human GRCh38 chr3: 141,051,201-141,201,000 , GRCh37.p13 chr3: 140,770,043-140,919,842 SPSB4
    nsv6725427copy number variation1nstd229human GRCh38 chr3: 141,101,266-141,131,244 , GRCh37.p13 chr3: 140,820,108-140,850,086 SPSB4
    nsv6723679copy number variation1nstd229human GRCh38 chr3: 141,109,347-141,109,640 , GRCh37.p13 chr3: 140,828,189-140,828,482 SPSB4
    nsv6723588copy number variation1nstd229human GRCh38 chr3: 141,062,836-141,062,992 , GRCh37.p13 chr3: 140,781,678-140,781,834 SPSB4
    nsv6723543copy number variation1nstd229human GRCh38 chr3: 141,110,139-141,149,981 , GRCh37.p13 chr3: 140,828,981-140,868,823 SPSB4
    nsv6723088copy number variation1nstd229human GRCh38 chr3: 141,001,081-141,158,392 , GRCh37.p13 chr3: 140,719,923-140,877,234 SPSB4
    nsv6721587copy number variation1nstd229human GRCh38 chr3: 141,144,333-141,147,703 , GRCh37.p13 chr3: 140,863,175-140,866,545 SPSB4
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