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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066313inversion1nstd229human GRCh38 chr11: 6,624,146-15,294,249 , GRCh37.p13 chr11: 6,645,377-15,315,795 RNA5SP332, TMEM41B, 163 more genes
    nsv7061813inversion1nstd229human GRCh38 chr11: 10,527,366-10,527,540 , GRCh37.p13 chr11: 10,548,913-10,549,087 RNF141
    nsv6917151copy number variation1nstd229human GRCh38 chr11: 9,940,109-18,580,574 , GRCh37.p13 chr11: 9,961,656-18,602,121 MYOD1, MIR8070, 139 more genes
    nsv6914840copy number variation1nstd229human GRCh38 chr11: 10,522,685-10,535,333 , GRCh37.p13 chr11: 10,544,232-10,556,880 RNF141
    nsv6910121copy number variation1nstd229human GRCh38 chr11: 10,522,891-10,530,276 , GRCh37.p13 chr11: 10,544,438-10,551,823 RNF141
    nsv6903829copy number variation1nstd229human GRCh38 chr11: 10,489,510-10,517,566 , GRCh37.p13 chr11: 10,511,057-10,539,113 RNF141, MIR4485, 2 more genes
    nsv6620945copy number variation1nstd224human GRCh37 chr11: 10,514,916-10,536,298 , GRCh38.p12 chr11: 10,493,369-10,514,751 MTRNR2L8, RNF141, 2 more genes
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6450885copy number variation1nstd223human GRCh38 chr11: 10,539,801-10,544,400 , GRCh37.p13 chr11: 10,561,348-10,565,947 IRAG1-AS1, RNF141
    nsv6450233copy number variation1nstd223human GRCh38 chr11: 10,522,685-10,535,333 , GRCh37.p13 chr11: 10,544,232-10,556,880 RNF141
    nsv6438588copy number variation1nstd223human GRCh38 chr11: 10,514,685-10,516,565 , GRCh37.p13 chr11: 10,536,232-10,538,112 RNF141
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6247765mobile element insertion1nstd215human GRCh38 chr11: 10,524,997-10,524,997 , GRCh37.p13 chr11: 10,546,544-10,546,544 RNF141
    nsv6099628insertion1nstd212human GRCh38 chr11: 10,539,699-10,539,699 , GRCh37.p13 chr11: 10,561,246-10,561,246 IRAG1-AS1, RNF141
    nsv6036596copy number variation1nstd212human GRCh38 chr11: 10,489,510-10,517,568 , GRCh37.p13 chr11: 10,511,057-10,539,115 AMPD3, RNF141, 2 more genes
    nsv5978402insertion1nstd209human GRCh38 chr11: 10,539,699-10,539,699 , GRCh37.p13 chr11: 10,561,246-10,561,246 RNF141, IRAG1-AS1
    nsv5646958insertion1nstd207human GRCh38 chr11: 10,527,459-10,527,459 , GRCh37.p13 chr11: 10,549,006-10,549,006 RNF141
    nsv5499463copy number variation1nstd206human GRCh38 chr11: 10,441,892-10,512,161 , GRCh37.p13 chr11: 10,463,439-10,533,708 RNF141, MTRNR2L8, 2 more genes
    nsv5344516translocation1nstd200human GRCh37 chr11: 10,555,562-10,555,562 , GRCh37 chr11: 10,552,298-10,552,298 , GRCh38.p12 chr11: 10,530,751-10,530,751 , GRCh38.p12 chr11: 10,534,015-10,534,015 RNF141
    nsv5242359copy number variation1nstd204human GRCh38.p13 chr11: 10,526,148-10,528,497 , GRCh37.p13 chr11: 10,547,695-10,550,044 RNF141
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