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Items: 1 to 20 of 577

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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
    nsv5949162insertion1nstd209human GRCh38 chr6: 136,414,252-136,414,252 , GRCh37.p13 chr6: 136,735,390-136,735,390 MAP7
    nsv5903566copy number variation1nstd209human GRCh38 chr6: 136,397,744-136,397,843 , GRCh37.p13 chr6: 136,718,882-136,718,981 MAP7
    nsv5903207copy number variation1nstd209human GRCh38 chr6: 136,505,287-136,506,621 , GRCh37.p13 chr6: 136,826,425-136,827,759 MAP7
    nsv5902933copy number variation1nstd209human GRCh38 chr6: 136,540,252-136,543,876 , GRCh37.p13 chr6: 136,861,390-136,865,014 RN7SKP299, MAP7
    nsv5901194copy number variation1nstd209human GRCh38 chr6: 136,414,483-136,418,936 , GRCh37.p13 chr6: 136,735,621-136,740,074 , MAP7
    nsv5893182copy number variation1nstd209human GRCh38 chr6: 136,496,381-136,500,114 , GRCh37.p13 chr6: 136,817,519-136,821,252 MAP7
    nsv5892308copy number variation1nstd209human GRCh38 chr6: 136,530,537-136,531,784 , GRCh37.p13 chr6: 136,851,675-136,852,922 MAP7
    nsv5888121copy number variation1nstd209human GRCh38 chr6: 136,508,082-136,508,215 , GRCh37.p13 chr6: 136,829,220-136,829,353 MAP7
    nsv5844387copy number variation1nstd209human GRCh38 chr6: 136,496,717-136,500,142 , GRCh37.p13 chr6: 136,817,855-136,821,280 MAP7
    nsv5844386copy number variation1nstd209human GRCh38 chr6: 136,414,519-136,418,918 , GRCh37.p13 chr6: 136,735,657-136,740,056 , MAP7
    nsv5844297copy number variation1nstd209human GRCh38 chr6: 136,540,381-136,543,905 , GRCh37.p13 chr6: 136,861,519-136,865,043 RN7SKP299, MAP7
    nsv5843766copy number variation1nstd209human GRCh38 chr6: 136,530,504-136,531,803 , GRCh37.p13 chr6: 136,851,642-136,852,941 MAP7
    nsv5688820mobile element insertion2nstd211human GRCh38 chr6: 136,492,773-136,492,773 , GRCh37.p13 chr6: 136,813,911-136,813,911 MAP7
    nsv5688164mobile element insertion2nstd211human GRCh38 chr6: 136,443,421-136,443,421 , GRCh37.p13 chr6: 136,764,559-136,764,559 MAP7
    nsv5686904mobile element insertion1nstd211human GRCh38 chr6: 136,422,717-136,422,717 , GRCh37.p13 chr6: 136,743,855-136,743,855 MAP7
    nsv5684885mobile element insertion2nstd211human GRCh38 chr6: 136,379,347-136,379,347 , GRCh37.p13 chr6: 136,700,485-136,700,485 MAP7
    nsv5683602mobile element insertion1nstd211human GRCh38 chr6: 136,546,015-136,546,015 , GRCh37.p13 chr6: 136,867,153-136,867,153 MAP7
    nsv5678851mobile element insertion2nstd211human GRCh38 chr6: 136,528,896-136,528,896 , GRCh37.p13 chr6: 136,850,034-136,850,034 MAP7
    nsv5678398mobile element insertion1nstd211human GRCh38 chr6: 136,481,409-136,481,409 , GRCh37.p13 chr6: 136,802,547-136,802,547 MAP7
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