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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054281inversion1nstd229human GRCh38 chr6: 137,136,591-137,147,017 , GRCh37.p13 chr6: 137,457,728-137,468,154 IL22RA2
    nsv7050559inversion1nstd229human GRCh38 chr6: 137,097,512-142,245,470 , GRCh37.p13 chr6: 137,418,649-142,566,607 LINC03004, LOC107986651, 64 more genes
    nsv7047763inversion1nstd229human GRCh38 chr6: 137,155,123-137,607,773 , GRCh37.p13 chr6: 137,476,260-137,928,910 IFNGR1, IL22RA2, 4 more genes
    nsv7043077inversion1nstd229human GRCh38 chr6: 137,166,718-137,166,830 , GRCh37.p13 chr6: 137,487,855-137,487,967 IL22RA2
    nsv7040605inversion1nstd229human GRCh38 chr6: 137,148,143-137,148,208 , GRCh37.p13 chr6: 137,469,280-137,469,345 IL22RA2
    nsv6811385copy number variation1nstd229human GRCh38 chr6: 137,153,662-137,157,067 , GRCh37.p13 chr6: 137,474,799-137,478,204 IL22RA2
    nsv6811018copy number variation1nstd229human GRCh38 chr6: 137,160,301-137,163,400 , GRCh37.p13 chr6: 137,481,438-137,484,537 IL22RA2
    nsv6803028copy number variation1nstd229human GRCh38 chr6: 137,171,688-137,171,884 , GRCh37.p13 chr6: 137,492,825-137,493,021 IL22RA2
    nsv6802969copy number variation1nstd229human GRCh38 chr6: 137,083,425-137,169,566 , GRCh37.p13 chr6: 137,404,562-137,490,703 IL22RA2
    nsv6802855copy number variation1nstd229human GRCh38 chr6: 137,145,412-137,149,434 , GRCh37.p13 chr6: 137,466,549-137,470,571 IL22RA2
    nsv6799666copy number variation1nstd229human GRCh38 chr6: 137,158,868-137,163,127 , GRCh37.p13 chr6: 137,480,005-137,484,264 IL22RA2
    nsv6600234copy number variation1nstd223human GRCh38 chr6: 137,160,286-137,163,439 , GRCh37.p13 chr6: 137,481,423-137,484,576 IL22RA2
    nsv6560305inversion1nstd223human GRCh38 chr6: 137,146,041-137,146,716 , GRCh37.p13 chr6: 137,467,178-137,467,853 IL22RA2
    nsv6314818copy number variation1nstd102humanPathogenic GRCh38 chr6: 134,838,331-142,160,056 , GRCh37.p13 chr6: 135,159,469-142,481,193 PBOV1, IFNGR1, 100 more genes
    nsv6312142copy number variation2nstd102humanPathogenic GRCh37 chr6: 137,143,759-138,202,456 , GRCh38.p12 chr6: 136,822,621-137,881,319 SLC35D3, LINC03004, 16 more genes
    nsv6112726copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,810,210-140,046,615 , GRCh38.p12 chr6: 133,489,072-139,725,478 SIMALR, MTFR2, 99 more genes
    nsv6010408copy number variation1nstd212human GRCh38 chr6: 137,083,422-137,169,565 , GRCh37.p13 chr6: 137,404,559-137,490,702 IL22RA2
    nsv5564202copy number variation1nstd102humanUncertain significance GRCh37 chr6: 137,143,759-137,540,520 , GRCh38.p12 chr6: 136,822,621-137,219,383 RPL35AP3, PEX7, 6 more genes
    nsv5469713copy number variation1nstd206human GRCh38 chr6: 137,150,167-137,150,260 , GRCh37.p13 chr6: 137,471,304-137,471,397 IL22RA2
    nsv5303899copy number variation1nstd204human GRCh38.p13 chr6: 136,677,049-137,315,602 , GRCh37.p13 chr6: 136,998,187-137,636,739 RPL35AP3, LOC105378017, 9 more genes
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