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Items: 1 to 20 of 94

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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
    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
    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
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    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
    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
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4672662copy number variation1nstd186human GRCh37 chr11: 10,529,488-10,534,969 , GRCh38.p12 chr11: 10,507,941-10,513,422 AMPD3, RNF141, 2 more genes
    nsv4665675copy number variation1nstd186human GRCh37 chr11: 10,529,348-10,531,585 , GRCh38.p12 chr11: 10,507,801-10,510,038 AMPD3, RNF141, 2 more genes
    nsv4609905copy number variation2nstd183human GRCh37 chr11: 10,529,348-10,531,585 , GRCh38.p12 chr11: 10,507,801-10,510,038 AMPD3, RNF141, 2 more genes
    nsv4607457copy number variation1nstd183human GRCh37 chr11: 10,529,055-10,531,585 , GRCh38.p12 chr11: 10,507,508-10,510,038 MIR4485, RNF141, 2 more genes
    nsv4602348copy number variation1nstd183human GRCh37 chr11: 10,529,470-10,531,983 , GRCh38.p12 chr11: 10,507,923-10,510,436 MTRNR2L8, AMPD3, 2 more genes
    nsv4599258copy number variation1nstd183human GRCh37 chr11: 10,529,488-10,534,969 , GRCh38.p12 chr11: 10,507,941-10,513,422 RNF141, MIR4485, 2 more genes
    nsv4415558copy number variation1nstd174human GRCh37 chr11: 10,529,039-10,532,011 , GRCh38.p12 chr11: 10,507,492-10,510,464 AMPD3, MTRNR2L8, 2 more genes
    nsv4367321copy number variation1nstd173human GRCh37 chr11: 9,422,923-11,175,143 , GRCh38.p12 chr11: 9,401,376-11,153,596 , LOC107984309, 40 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
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