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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5685678mobile element insertion2nstd211human GRCh38 chr6: 137,036,687-137,036,687 , GRCh37.p13 chr6: 137,357,824-137,357,824 IL20RA
    nsv5683612mobile element insertion2nstd211human GRCh38 chr6: 137,024,163-137,024,163 , GRCh37.p13 chr6: 137,345,300-137,345,300 IL20RA
    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
    nsv5406928mobile element insertion1nstd206human GRCh38 chr6: 137,024,163-137,024,214 , GRCh37.p13 chr6: 137,345,300-137,345,351 IL20RA
    nsv5398782mobile element insertion1nstd206human GRCh38 chr6: 137,036,687-137,036,738 , GRCh37.p13 chr6: 137,357,824-137,357,875 IL20RA
    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
    nsv5226311copy number variation1nstd204human GRCh38.p13 chr6: 136,974,882-137,006,374 , GRCh37.p13 chr6: 137,296,019-137,327,511 NHEG1, IL20RA
    nsv5119946mobile element insertion1nstd203human GRCh38 chr6: 137,036,672-137,036,687 , GRCh37.p13 chr6: 137,357,809-137,357,824 IL20RA
    nsv4945718copy number variation1nstd200human GRCh38 chr6: 137,034,586-137,260,679 , GRCh37.p13 chr6: 137,355,723-137,581,816 IFNGR1, IL22RA2, 1 more genes
    nsv4942880copy number variation1nstd200human GRCh38 chr6: 136,998,506-136,998,713 , GRCh37.p13 chr6: 137,319,643-137,319,850 IL20RA
    nsv4810550copy number variation1nstd200human GRCh37 chr6: 137,326,650-137,336,459 , GRCh38.p12 chr6: 137,005,513-137,015,322 IL20RA
    nsv4685709copy number variation1nstd102humannot provided GRCh37 chr6: 135,936,688-140,660,269 , GRCh38.p12 chr6: 135,615,550-140,339,132 MAP7, RN7SKP299, 74 more genes
    nsv4683010copy number variation1nstd102humanPathogenic GRCh37 chr6: 136,482,728-137,540,520 , GRCh38.p12 chr6: 136,161,590-137,219,383 PDE7B, RN7SKP299, 17 more genes
    nsv4675250copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,817,341-140,038,401 , GRCh38.p12 chr6: 133,496,203-139,717,264 ALDH8A1, IL22RA2, 99 more genes
    nsv4556823insertion1nstd166human GRCh37.p13 chr6: 137,357,809-137,357,809 , GRCh38.p12 chr6: 137,036,672-137,036,672 IL20RA
    nsv4547868insertion1nstd166human GRCh37.p13 chr6: 137,339,470-137,339,470 , GRCh38.p12 chr6: 137,018,333-137,018,333 IL20RA
    nsv4350212copy number variation1nstd102humanPathogenic GRCh37 chr6: 135,239,633-146,997,510 , GRCh38.p12 chr6: 134,918,495-146,676,374 LOC100131041, ADGB-DT, 146 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
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