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Items: 1 to 20 of 130

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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
    nsv5535770insertion1nstd206human GRCh38 chr6: 135,181,137-135,181,158 , GRCh37.p13 chr6: 135,502,275-135,502,296 MYB
    nsv5472145copy number variation1nstd206human GRCh38 chr6: 135,205,074-135,206,169 , GRCh37.p13 chr6: 135,526,212-135,527,307 LOC105378011, MYB
    nsv4826572copy number variation1nstd200human GRCh37 chr6: 135,503,691-135,503,896 , GRCh38.p12 chr6: 135,182,553-135,182,758 MYB
    nsv4675250copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,817,341-140,038,401 , GRCh38.p12 chr6: 133,496,203-139,717,264 ALDH8A1, IL22RA2, 99 more genes
    nsv4606001copy number variation1nstd183human GRCh37 chr6: 135,528,488-135,557,305 , GRCh38.p12 chr6: 135,207,350-135,236,167 LOC105378011, MYB
    nsv4565050mobile element insertion1nstd166human GRCh37.p13 chr6: 135,518,662-135,518,662 , GRCh38.p12 chr6: 135,197,524-135,197,524 LOC105378011, MYB
    nsv4542807insertion1nstd166human GRCh37.p13 chr6: 135,502,245-135,502,245 , GRCh38.p12 chr6: 135,181,107-135,181,107 MYB
    nsv4524826copy number variation1nstd166human GRCh37.p13 chr6: 135,526,922-135,527,345 , GRCh38.p12 chr6: 135,205,784-135,206,207 LOC105378011, MYB
    nsv4350212copy number variation1nstd102humanPathogenic GRCh37 chr6: 135,239,633-146,997,510 , GRCh38.p12 chr6: 134,918,495-146,676,374 LOC100131041, ADGB-DT, 146 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv4144137copy number variation1nstd166human GRCh37.p13 chr6: 135,523,068-135,524,175 , GRCh38.p12 chr6: 135,201,930-135,203,037 LOC105378011, MYB
    nsv4142290copy number variation1nstd166human GRCh37.p13 chr6: 135,533,181-135,533,388 , GRCh38.p12 chr6: 135,212,043-135,212,250 LOC105378011, MYB
    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
    nsv3913689copy number variation1nstd102humanPathogenic NCBI36 chr6: 121,373,749-146,289,101 , GRCh37.p13 chr6: 121,332,050-146,247,408 , GRCh38.p12 chr6: 121,010,904-145,926,272 TPD52L1, MESTP1, 316 more genes
    nsv3911993copy number variation1nstd102humanPathogenic NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033 LOC105369171, SHPRH, 418 more genes
    nsv3904441copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,077,239-143,761,582 , GRCh38.p12 chr6: 132,756,100-143,440,445 SNORD101, MTFR2, 147 more genes
    nsv3893875copy number variation1nstd102humanPathogenic GRCh37 chr6: 132,002,460-137,160,850 , GRCh38.p12 chr6: 131,681,320-136,839,712 TAAR9, EEF1A1P36, 93 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
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