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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974647inversion1nstd209human GRCh38 chr6: 127,434,769-127,509,002 , GRCh37.p13 chr6: 127,755,914-127,830,147 KIAA0408, MTCL3, 2 more genes
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5906945copy number variation1nstd209human GRCh38 chr6: 123,301,756-132,349,395 , GRCh37.p13 chr6: 123,622,901-132,670,534 , LOC105377999, 105 more genes
    nsv5894472copy number variation1nstd209human GRCh38 chr6: 127,447,593-127,447,645 , GRCh37.p13 chr6: 127,768,738-127,768,790 KIAA0408, MTCL3
    nsv5680851mobile element insertion2nstd211human GRCh38 chr6: 127,456,854-127,456,854 , GRCh37.p13 chr6: 127,777,999-127,777,999 MTCL3, KIAA0408
    nsv5403904mobile element insertion1nstd206human GRCh38 chr6: 127,456,854-127,456,905 , GRCh37.p13 chr6: 127,777,999-127,778,050 MTCL3, KIAA0408
    nsv5300854copy number variation1nstd204human GRCh37.p13 chr6: 127,766,902-127,767,995 , GRCh38.p13 chr6: 127,445,757-127,446,850 KIAA0408, MTCL3
    nsv5228791copy number variation1nstd204human GRCh38.p13 chr6: 127,445,253-127,446,902 , GRCh37.p13 chr6: 127,766,398-127,768,047 KIAA0408, MTCL3
    nsv5224688copy number variation1nstd204human GRCh38.p13 chr6: 127,445,801-127,446,800 , GRCh37.p13 chr6: 127,766,946-127,767,945 KIAA0408, MTCL3
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4826381copy number variation1nstd200human GRCh37 chr6: 127,766,925-127,767,972 , GRCh38.p12 chr6: 127,445,780-127,446,827 KIAA0408, MTCL3
    nsv4599483copy number variation2nstd183human GRCh37 chr6: 127,758,469-127,762,930 , GRCh38.p12 chr6: 127,437,324-127,441,785 MTCL3, KIAA0408
    nsv4572762sequence alteration1nstd166human GRCh37.p13 chr6: 127,763,712-127,764,598 , GRCh38.p12 chr6: 127,442,567-127,443,453 KIAA0408, MTCL3
    nsv4496571mobile element insertion1nstd166human GRCh37.p13 chr6: 127,777,985-127,777,985 , GRCh38.p12 chr6: 127,456,840-127,456,840 MTCL3, KIAA0408
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv3924661copy number variation1nstd102humanPathogenic GRCh38 chr6: 115,601,230-128,514,324 , GRCh37 chr6: 115,922,394-128,835,469 , NCBI36 chr6: 116,029,087-128,877,162 MCM9, YWHAZP4, 146 more genes
    nsv3922290copy number variation1nstd102humanUncertain significance GRCh37 chr6: 125,342,919-128,092,979 , GRCh38 chr6: 125,021,773-127,771,834 , NCBI36 chr6: 125,384,618-128,134,672 THEMIS, PPP1R14BP5, 45 more genes
    nsv3920683copy number variation1nstd102humanPathogenic NCBI36 chr6: 109,372,795-132,430,553 , GRCh37 chr6: 109,266,102-132,388,860 , GRCh38 chr6: 108,944,899-132,067,720 SSXP10, TRE-CTC1-7, 298 more genes
    nsv3919111copy number variation1nstd102humanPathogenic GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637 RNU6-770P, MAP3K5-AS2, 810 more genes
    nsv3915150copy number variation1nstd102humanPathogenic NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038 KATNA1, RNF217-AS1, 422 more genes
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