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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5899267copy number variation1nstd209human GRCh38 chr6: 42,957,850-43,031,425 , GRCh37.p13 chr6: 42,925,588-42,999,163 MEA1, PEX6, 5 more genes
    nsv5844903copy number variation1nstd209human GRCh38 chr6: 42,957,892-42,976,087 , GRCh37.p13 chr6: 42,925,630-42,943,825 GNMT, CNPY3-GNMT, 1 more genes
    nsv5673767copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 42,931,601-42,937,735 , GRCh38.p12 chr6: 42,963,863-42,969,997 PEX6, GNMT, 1 more genes
    nsv5673766copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,928,506-43,737,486 , GRCh38.p12 chr6: 42,960,768-43,769,749 SRF, POLR1C, 39 more genes
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5381625copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,928,506-42,952,462 , GRCh38.p12 chr6: 42,960,768-42,984,724 PEX6, PPP2R5D, 3 more genes
    nsv5237511copy number variation1nstd204human GRCh38.p13 chr6: 42,950,601-42,978,700 , GRCh37.p13 chr6: 42,918,339-42,946,438 GNMT, MEA1, 3 more genes
    nsv5237305copy number variation1nstd204human GRCh38.p13 chr6: 42,950,719-42,970,329 , GRCh37.p13 chr6: 42,918,457-42,938,067 GNMT, PEX6, 2 more genes
    nsv5224950copy number variation1nstd204human GRCh38.p13 chr6: 42,543,301-43,041,600 , GRCh37.p13 chr6: 42,511,039-43,009,338 , RPL7L1, 20 more genes
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4682355copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,890,765-42,952,442 , GRCh38.p12 chr6: 42,923,027-42,984,704 MEA1, CNPY3-GNMT, 6 more genes
    nsv4592683copy number variation1nstd183human GRCh37 chr6: 42,627,455-43,357,404 , GRCh38.p12 chr6: 42,659,717-43,389,666 , PEX6, 36 more genes
    nsv4456164copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,903,316-42,955,264 , GRCh38.p12 chr6: 42,935,578-42,987,526 RPL24P4, CNPY3, 5 more genes
    nsv4455583copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,903,316-42,954,083 , GRCh38.p12 chr6: 42,935,578-42,986,345 MEA1, CNPY3-GNMT, 5 more genes
    nsv4369718copy number variation1nstd173human GRCh37 chr6: 42,882,476-42,953,200 , GRCh38.p12 chr6: 42,914,738-42,985,462 RPL24P4, PTCRA, 6 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv4147691copy number variation1nstd166human GRCh37.p13 chr6: 42,908,197-42,954,908 , GRCh38.p12 chr6: 42,940,459-42,987,170 MEA1, PEX6, 4 more genes
    nsv3924318copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,336,296-44,558,281 , NCBI36 chr6: 42,444,274-44,666,259 , GRCh38 chr6: 42,368,558-44,590,544 MIR4642, SRF, 82 more genes
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