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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5633832insertion1nstd207human GRCh38 chr6: 125,962,189-125,962,189 , GRCh37.p13 chr6: 126,283,335-126,283,335 HINT3
    nsv5584365copy number variation1nstd207human GRCh38 chr6: 125,962,219-125,962,274 , GRCh37.p13 chr6: 126,283,365-126,283,420 HINT3
    nsv5579608copy number variation1nstd207human GRCh38 chr6: 125,962,185-125,962,311 , GRCh37.p13 chr6: 126,283,331-126,283,457 HINT3
    nsv5464563copy number variation1nstd206human GRCh38 chr6: 125,971,498-125,971,575 , GRCh37.p13 chr6: 126,292,644-126,292,721 HINT3
    nsv5333727translocation1nstd200human GRCh37 chr6: 126,292,721-126,292,721 , GRCh37 chr6: 126,292,644-126,292,644 , GRCh38.p12 chr6: 125,971,498-125,971,498 , GRCh38.p12 chr6: 125,971,575-125,971,575 HINT3
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4933959copy number variation1nstd200human GRCh38 chr6: 125,971,305-126,009,213 , GRCh37.p13 chr6: 126,292,451-126,330,359 RNA5SP216, TRMT11, 1 more genes
    nsv4732917copy number variation1nstd199human GRCh37 chr6: 126,283,305-126,283,365 , GRCh38.p12 chr6: 125,962,159-125,962,219 HINT3
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv4144670copy number variation1nstd166human GRCh37.p13 chr6: 126,282,797-126,283,460 , GRCh38.p12 chr6: 125,961,651-125,962,314 HINT3
    nsv4142464copy number variation1nstd166human GRCh37.p13 chr6: 126,276,010-126,319,603 , GRCh38.p12 chr6: 125,954,864-125,998,457 RNA5SP216, TRMT11, 1 more genes
    nsv3929632copy number variation1nstd167human GRCh37 chr6: 126,283,401-126,283,461 , GRCh38.p12 chr6: 125,962,255-125,962,315 HINT3
    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
    nsv3924512copy number variation1nstd102humanPathogenic NCBI36 chr6: 118,035,003-127,062,818 , GRCh37 chr6: 117,928,310-127,021,125 , GRCh38 chr6: 117,607,147-126,699,980 HSF2, LOC285762, 85 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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