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Items: 1 to 20 of 653

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5951382insertion1nstd209human GRCh38 chr6: 146,180,181-146,180,181 , GRCh37.p13 chr6: 146,501,317-146,501,317 GRM1
    nsv5907027copy number variation1nstd209human GRCh38 chr6: 146,225,677-146,238,070 , GRCh37.p13 chr6: 146,546,813-146,559,206 GRM1
    nsv5895333copy number variation1nstd209human GRCh38 chr6: 146,212,766-146,213,076 , GRCh37.p13 chr6: 146,533,902-146,534,212 GRM1
    nsv5889105copy number variation1nstd209human GRCh38 chr6: 146,086,135-146,087,124 , GRCh37.p13 chr6: 146,407,271-146,408,260 GRM1
    nsv5844637copy number variation1nstd209human GRCh38 chr6: 146,086,156-146,087,155 , GRCh37.p13 chr6: 146,407,292-146,408,291 GRM1
    nsv5844068copy number variation1nstd209human GRCh38 chr6: 146,225,623-146,238,097 , GRCh37.p13 chr6: 146,546,759-146,559,233 GRM1
    nsv5693277mobile element insertion1nstd211human GRCh38 chr6: 146,218,140-146,218,140 , GRCh37.p13 chr6: 146,539,276-146,539,276 GRM1
    nsv5692537mobile element insertion1nstd211human GRCh38 chr6: 146,324,914-146,324,914 , GRCh37.p13 chr6: 146,646,050-146,646,050 GRM1
    nsv5692355mobile element insertion2nstd211human GRCh38 chr6: 146,369,559-146,369,559 , GRCh37.p13 chr6: 146,690,695-146,690,695 GRM1
    nsv5691743mobile element insertion2nstd211human GRCh38 chr6: 146,115,175-146,115,175 , GRCh37.p13 chr6: 146,436,311-146,436,311 GRM1
    nsv5691344mobile element insertion2nstd211human GRCh38 chr6: 146,199,711-146,199,711 , GRCh37.p13 chr6: 146,520,847-146,520,847 GRM1
    nsv5685023mobile element insertion2nstd211human GRCh38 chr6: 146,391,112-146,391,112 , GRCh37.p13 chr6: 146,712,248-146,712,248 GRM1
    nsv5684525mobile element insertion1nstd211human GRCh38 chr6: 146,253,620-146,253,620 , GRCh37.p13 chr6: 146,574,756-146,574,756 GRM1
    nsv5680946mobile element insertion2nstd211human GRCh38 chr6: 146,180,194-146,180,194 , GRCh37.p13 chr6: 146,501,330-146,501,330 GRM1
    nsv5680879mobile element insertion1nstd211human GRCh38 chr6: 146,121,515-146,121,515 , GRCh37.p13 chr6: 146,442,651-146,442,651 GRM1
    nsv5676231mobile element insertion1nstd211human GRCh38 chr6: 146,345,947-146,345,947 , GRCh37.p13 chr6: 146,667,083-146,667,083 GRM1
    nsv5675549mobile element insertion2nstd211human GRCh38 chr6: 146,301,033-146,301,033 , GRCh37.p13 chr6: 146,622,169-146,622,169 GRM1
    nsv5628237insertion1nstd207human GRCh38 chr6: 146,180,181-146,180,181 , GRCh37.p13 chr6: 146,501,317-146,501,317 GRM1
    nsv5625412insertion1nstd207human GRCh38 chr6: 146,237,441-146,237,441 , GRCh37.p13 chr6: 146,558,577-146,558,577 GRM1
    nsv5561598sequence alteration1nstd206human GRCh38 chr6: 146,085,439-146,086,528 , GRCh37.p13 chr6: 146,406,575-146,407,664 GRM1
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