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Items: 1 to 20 of 120

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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
    nsv5693201mobile element insertion1nstd211human GRCh38 chr6: 136,629,795-136,629,795 , GRCh37.p13 chr6: 136,950,933-136,950,933 MAP3K5, RNA5SP219, 1 more genes
    nsv5678165mobile element insertion1nstd211human GRCh38 chr6: 136,633,981-136,633,981 , GRCh37.p13 chr6: 136,955,119-136,955,119 MAP3K5, MAP3K5-AS1
    nsv5403947mobile element insertion1nstd206human GRCh38 chr6: 136,633,981-136,634,032 , GRCh37.p13 chr6: 136,955,119-136,955,170 MAP3K5-AS1, MAP3K5
    nsv4685709copy number variation1nstd102humannot provided GRCh37 chr6: 135,936,688-140,660,269 , GRCh38.p12 chr6: 135,615,550-140,339,132 MAP7, RN7SKP299, 74 more genes
    nsv4683010copy number variation1nstd102humanPathogenic GRCh37 chr6: 136,482,728-137,540,520 , GRCh38.p12 chr6: 136,161,590-137,219,383 PDE7B, RN7SKP299, 17 more genes
    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
    nsv4486166mobile element insertion1nstd166human GRCh37.p13 chr6: 136,955,103-136,955,103 , GRCh38.p12 chr6: 136,633,965-136,633,965 MAP3K5-AS1, MAP3K5
    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
    nsv4152131copy number variation1nstd166human GRCh37.p13 chr6: 136,956,889-136,957,434 , GRCh38.p12 chr6: 136,635,751-136,636,296 MAP3K5, MAP3K5-AS1
    nsv3919212copy number variation1nstd102humanUncertain significance NCBI36 chr6: 136,454,132-138,137,046 , GRCh37.p13 chr6: 136,412,439-138,095,353 , GRCh38.p12 chr6: 136,091,301-137,774,216 MAP3K5-AS1, LOC102723633, 25 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
    nsv3916499copy number variation1nstd102humanPathogenic NCBI36 chr6: 136,359,437-146,708,473 , GRCh37.p13 chr6: 136,317,744-146,666,780 , GRCh38.p12 chr6: 135,996,606-146,345,644 SLC35D3, SHPRH, 127 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
    nsv3911251copy number variation1nstd102humanLikely benign GRCh38 chr6: 136,630,655-137,791,240 , NCBI36 chr6: 136,993,486-138,154,070 , GRCh37 chr6: 136,951,793-138,112,377 SLC35D3, IL22RA2, 18 more genes
    nsv3911164copy number variation1nstd102humanPathogenic NCBI36 chr6: 135,720,981-155,817,943 , GRCh37 chr6: 135,679,288-155,776,251 , GRCh38 chr6: 135,358,150-155,455,117 HYMAI, SMIM28, 263 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
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