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Items: 1 to 20 of 104

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047023inversion1nstd229human GRCh38 chr6: 136,925,152-136,925,163 , GRCh37.p13 chr6: 137,246,290-137,246,301 SLC35D3
    nsv6807354copy number variation1nstd229human GRCh38 chr6: 136,437,522-136,955,719 , GRCh37.p13 chr6: 136,758,660-137,276,857 MAP3K5-AS2, RN7SKP299, 8 more genes
    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
    nsv6135474copy number variation1nstd213human GRCh37 chr6: 136,910,000-137,260,001 , GRCh38.p12 chr6: 136,588,862-136,938,863 MAP3K5, PEX7, 5 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
    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
    nsv5333893translocation1nstd200human GRCh37 chr6: 137,245,990-137,245,990 , GRCh37 chr6: 137,248,640-137,248,640 , GRCh38.p12 chr6: 136,924,852-136,924,852 , GRCh38.p12 chr6: 136,927,502-136,927,502 SLC35D3
    nsv5333792translocation1nstd200human GRCh37 chr6: 137,246,087-137,246,087 , GRCh37 chr6: 137,245,964-137,245,964 , GRCh38.p12 chr6: 136,924,826-136,924,826 , GRCh38.p12 chr6: 136,924,949-136,924,949 SLC35D3
    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
    nsv4942876copy number variation1nstd200human GRCh38 chr6: 136,924,825-136,927,501 , GRCh37.p13 chr6: 137,245,963-137,248,639 SLC35D3
    nsv4810547copy number variation1nstd200human GRCh37 chr6: 137,245,963-137,248,639 , GRCh38.p12 chr6: 136,924,825-136,927,501 SLC35D3
    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
    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
    nsv4152324copy number variation1nstd166human GRCh37.p13 chr6: 137,139,061-137,264,171 , GRCh38.p12 chr6: 136,817,923-136,943,033 PEX7, RPL7AP37, 1 more genes
    nsv4134227copy number variation1nstd166human GRCh37.p13 chr6: 137,245,964-137,248,639 , GRCh38.p12 chr6: 136,924,826-136,927,501 SLC35D3
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