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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6794101copy number variation1nstd229human GRCh38 chr6: 44,281,787-44,286,069 , GRCh37.p13 chr6: 44,249,524-44,253,806 TCTE1
    nsv6788779copy number variation1nstd229human GRCh38 chr6: 44,217,191-44,323,601 , GRCh37.p13 chr6: 44,184,928-44,291,338 TMEM151B, TCTE1, 7 more genes
    nsv6787929copy number variation1nstd229human GRCh38 chr6: 44,278,416-44,278,614 , GRCh37.p13 chr6: 44,246,153-44,246,351 TMEM151B, TCTE1
    nsv6787193copy number variation1nstd229human GRCh38 chr6: 44,181,401-44,326,600 , GRCh37.p13 chr6: 44,149,138-44,294,337 TMEM151B, AARS2, 10 more genes
    nsv6781156copy number variation1nstd229human GRCh38 chr6: 44,296,642-44,296,673 , GRCh37.p13 chr6: 44,264,379-44,264,410 TCTE1, AARS2
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv6135515copy number variation1nstd213human GRCh37 chr6: 43,220,000-44,970,001 , GRCh38.p12 chr6: 43,252,262-45,002,264 SLC29A1, NFKBIE, 54 more genes
    nsv6119728copy number variation1nstd186human GRCh37 chr6: 44,264,681-44,264,732 , GRCh38.p12 chr6: 44,296,944-44,296,995 TCTE1, AARS2
    nsv6066490insertion1nstd212human GRCh38 chr6: 44,296,969-44,296,969 , GRCh37.p13 chr6: 44,264,706-44,264,706 AARS2, TCTE1
    nsv5948897insertion1nstd209human GRCh38 chr6: 44,296,935-44,296,935 , GRCh37.p13 chr6: 44,264,672-44,264,672 AARS2, TCTE1
    nsv5642251insertion1nstd207human GRCh38 chr6: 44,296,939-44,296,939 , GRCh37.p13 chr6: 44,264,676-44,264,676 AARS2, TCTE1
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5456570copy number variation1nstd206human GRCh38 chr6: 44,296,944-44,296,995 , GRCh37.p13 chr6: 44,264,681-44,264,732 TCTE1, AARS2
    nsv4934690copy number variation1nstd200human GRCh38 chr6: 44,278,416-44,278,615 , GRCh37.p13 chr6: 44,246,153-44,246,352 TCTE1, TMEM151B
    nsv4816219copy number variation1nstd200human GRCh37 chr6: 44,253,068-44,253,772 , GRCh38.p12 chr6: 44,285,331-44,286,035 TCTE1
    nsv4763773insertion1nstd199human GRCh37 chr6: 44,264,671-44,264,671 , GRCh38.p12 chr6: 44,296,934-44,296,934 AARS2, TCTE1
    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
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