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Items: 1 to 20 of 139

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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
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6909430copy number variation1nstd229human GRCh38 chr11: 8,911,101-8,979,500 , GRCh37.p13 chr11: 8,932,648-9,001,047 C11orf16, ASCL3, 5 more genes
    nsv6906971copy number variation1nstd229human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 RIC3, LOC644656, 86 more genes
    nsv6905931copy number variation1nstd229human GRCh38 chr11: 8,963,801-8,965,600 , GRCh37.p13 chr11: 8,985,348-8,987,147 TMEM9B, TMEM9B-AS1
    nsv6901097copy number variation1nstd229human GRCh38 chr11: 8,567,643-8,968,110 , GRCh37.p13 chr11: 8,589,190-8,989,657 SNORA3B, RPL27A, 12 more genes
    nsv6621031copy number variation1nstd224human GRCh37 chr11: 8,959,020-8,970,008 , GRCh38.p12 chr11: 8,937,473-8,948,461 TMEM9B, ASCL3
    nsv6585004inversion1nstd223human GRCh38 chr11: 8,958,290-8,958,649 , GRCh37.p13 chr11: 8,979,837-8,980,196 TMEM9B
    nsv6581885inversion1nstd223human GRCh38 chr11: 8,954,447-8,955,123 , GRCh37.p13 chr11: 8,975,994-8,976,670 TMEM9B
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6453605copy number variation1nstd223human GRCh38 chr11: 8,836,740-9,205,220 , GRCh37.p13 chr11: 8,858,287-9,226,767 MIR5691, LOC105376542, 12 more genes
    nsv6442855copy number variation1nstd223human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 LOC105369149, C11orf16, 86 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6030464copy number variation1nstd212human GRCh37.p13 chr11: 8,839,646-9,001,117 , GRCh38 chr11: 8,818,099-8,979,570 DENND2B, AKIP1, 6 more genes
    nsv6020879copy number variation1nstd212human GRCh37.p13 chr11: 8,839,663-8,998,871 , GRCh38 chr11: 8,818,116-8,977,324 DENND2B, AKIP1, 5 more genes
    nsv5916663copy number variation1nstd209human GRCh38 chr11: 8,818,116-8,977,319 , GRCh37.p13 chr11: 8,839,663-8,998,866 DENND2B, AKIP1, 5 more genes
    nsv5186673mobile element insertion1nstd203human GRCh38 chr11: 8,946,819-8,946,835 , GRCh37.p13 chr11: 8,968,366-8,968,382 TMEM9B
    nsv4978154copy number variation1nstd200human GRCh38 chr11: 8,956,387-8,965,268 , GRCh37.p13 chr11: 8,977,934-8,986,815 TMEM9B, TMEM9B-AS1
    nsv4978153copy number variation1nstd200human GRCh38 chr11: 8,953,685-8,953,790 , GRCh37.p13 chr11: 8,975,232-8,975,337 TMEM9B
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
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