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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097813copy number variation1nstd102humanUncertain significance GRCh37 chr6: 137,519,168-137,528,234 , GRCh38.p12 chr6: 137,198,031-137,207,097 IFNGR1
    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
    nsv6817502copy number variation1nstd229human GRCh38 chr6: 137,204,170-137,204,764 , GRCh37.p13 chr6: 137,525,307-137,525,901 IFNGR1
    nsv6808156copy number variation1nstd229human GRCh38 chr6: 137,212,078-137,212,788 , GRCh37.p13 chr6: 137,533,215-137,533,925 IFNGR1
    nsv6805524copy number variation1nstd229human GRCh38 chr6: 137,192,680-137,205,811 , GRCh37.p13 chr6: 137,513,817-137,526,948 IFNGR1
    nsv6805160copy number variation1nstd229human GRCh38 chr6: 137,214,022-137,214,481 , GRCh37.p13 chr6: 137,535,159-137,535,618 IFNGR1
    nsv6610556copy number variation1nstd223human GRCh38 chr6: 137,216,738-137,217,160 , GRCh37.p13 chr6: 137,537,875-137,538,297 IFNGR1
    nsv6603252copy number variation1nstd223human GRCh38 chr6: 137,192,677-137,205,810 , GRCh37.p13 chr6: 137,513,814-137,526,947 IFNGR1
    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
    nsv6078689insertion1nstd212human GRCh38 chr6: 137,199,528-137,199,528 , GRCh37.p13 chr6: 137,520,665-137,520,665 IFNGR1
    nsv5693917mobile element insertion1nstd211human GRCh38 chr6: 137,209,962-137,209,962 , GRCh37.p13 chr6: 137,531,099-137,531,099 IFNGR1
    nsv5642369insertion1nstd207human GRCh38 chr6: 137,199,528-137,199,528 , GRCh37.p13 chr6: 137,520,665-137,520,665 IFNGR1
    nsv5627024insertion1nstd207human GRCh38 chr6: 137,199,459-137,199,459 , GRCh37.p13 chr6: 137,520,596-137,520,596 IFNGR1
    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
    nsv5401434mobile element insertion1nstd206human GRCh38 chr6: 137,209,962-137,210,013 , GRCh37.p13 chr6: 137,531,099-137,531,150 IFNGR1
    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
    nsv5239138copy number variation1nstd204human GRCh38.p13 chr6: 136,676,801-137,315,600 , GRCh37.p13 chr6: 136,997,939-137,636,737 MAP3K5-AS2, NHEG1, 9 more genes
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