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Items: 1 to 20 of 502

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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
    nsv5963067insertion1nstd209human GRCh38 chr6: 136,585,477-136,585,477 , GRCh37.p13 chr6: 136,906,615-136,906,615 MAP3K5
    nsv5957103insertion1nstd209human GRCh38 chr6: 136,737,041-136,737,041 , GRCh37.p13 chr6: 137,058,179-137,058,179 MAP3K5
    nsv5957024insertion1nstd209human GRCh38 chr6: 136,697,601-136,697,601 , GRCh37.p13 chr6: 137,018,739-137,018,739 MAP3K5
    nsv5905617copy number variation1nstd209human GRCh38 chr6: 136,554,407-136,555,358 , GRCh37.p13 chr6: 136,875,545-136,876,496 MAP3K5
    nsv5899423copy number variation1nstd209human GRCh38 chr6: 136,559,358-136,559,412 , GRCh37.p13 chr6: 136,880,496-136,880,550 MAP3K5
    nsv5729913mobile element insertion1nstd211human GRCh38 chr6: 136,705,504-136,705,504 , GRCh37.p13 chr6: 137,026,642-137,026,642 MAP3K5
    nsv5716942mobile element insertion2nstd211human GRCh38 chr6: 136,697,616-136,697,616 , GRCh37.p13 chr6: 137,018,754-137,018,754 MAP3K5
    nsv5694215mobile element insertion2nstd211human GRCh38 chr6: 136,704,079-136,704,079 , GRCh37.p13 chr6: 137,025,217-137,025,217 MAP3K5
    nsv5693201mobile element insertion1nstd211human GRCh38 chr6: 136,629,795-136,629,795 , GRCh37.p13 chr6: 136,950,933-136,950,933 MAP3K5, RNA5SP219, 1 more genes
    nsv5692225mobile element insertion1nstd211human GRCh38 chr6: 136,733,840-136,733,840 , GRCh37.p13 chr6: 137,054,978-137,054,978 MAP3K5
    nsv5682870mobile element insertion2nstd211human GRCh38 chr6: 136,660,982-136,660,982 , GRCh37.p13 chr6: 136,982,120-136,982,120 MAP3K5
    nsv5680036mobile element insertion1nstd211human GRCh38 chr6: 136,706,771-136,706,771 , GRCh37.p13 chr6: 137,027,909-137,027,909 MAP3K5
    nsv5678165mobile element insertion1nstd211human GRCh38 chr6: 136,633,981-136,633,981 , GRCh37.p13 chr6: 136,955,119-136,955,119 MAP3K5, MAP3K5-AS1
    nsv5634127insertion1nstd207human GRCh38 chr6: 136,737,041-136,737,041 , GRCh37.p13 chr6: 137,058,179-137,058,179 MAP3K5
    nsv5633665insertion1nstd207human GRCh38 chr6: 136,697,601-136,697,601 , GRCh37.p13 chr6: 137,018,739-137,018,739 MAP3K5
    nsv5628771insertion1nstd207human GRCh38 chr6: 136,585,469-136,585,469 , GRCh37.p13 chr6: 136,906,607-136,906,607 MAP3K5
    nsv5625780insertion1nstd207human GRCh38 chr6: 136,705,494-136,705,494 , GRCh37.p13 chr6: 137,026,632-137,026,632 MAP3K5
    nsv5576010copy number variation1nstd207human GRCh38 chr6: 136,559,358-136,559,412 , GRCh37.p13 chr6: 136,880,496-136,880,550 MAP3K5
    nsv5569912copy number variation1nstd207human GRCh38 chr6: 136,763,993-136,767,960 , GRCh37.p13 chr6: 137,085,131-137,089,098 MAP3K5
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