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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071548inversion1nstd229human GRCh38 chr11: 10,488,626-10,504,337 , GRCh37.p13 chr11: 10,510,173-10,525,884 AMPD3
    nsv7068148inversion1nstd229human GRCh38 chr11: 10,489,470-10,489,583 , GRCh37.p13 chr11: 10,511,017-10,511,130 AMPD3
    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
    nsv6899574copy number variation1nstd229human GRCh38 chr11: 10,458,102-10,459,425 , GRCh37.p13 chr11: 10,479,649-10,480,972 AMPD3
    nsv6898602copy number variation1nstd229human GRCh38 chr11: 10,474,722-10,478,555 , GRCh37.p13 chr11: 10,496,269-10,500,102 AMPD3
    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
    nsv6280143insertion1nstd214human GRCh38 chr11: 10,480,511-10,480,511 , GRCh37.p13 chr11: 10,502,058-10,502,058 AMPD3
    nsv6096508insertion1nstd212human GRCh38 chr11: 10,480,525-10,480,525 , GRCh37.p13 chr11: 10,502,072-10,502,072 AMPD3
    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
    nsv5697030mobile element insertion2nstd211human GRCh38 chr11: 10,448,917-10,448,917 , GRCh37.p13 chr11: 10,470,464-10,470,464 AMPD3
    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
    nsv5394000mobile element insertion1nstd206human GRCh38 chr11: 10,448,917-10,448,968 , GRCh37.p13 chr11: 10,470,464-10,470,515 AMPD3
    nsv5138379mobile element insertion1nstd203human GRCh38 chr11: 10,460,571-10,460,580 , GRCh37.p13 chr11: 10,482,118-10,482,127 AMPD3
    nsv5132366mobile element insertion1nstd203human GRCh38 chr11: 10,448,906-10,448,912 , GRCh37.p13 chr11: 10,470,453-10,470,459 AMPD3
    nsv5122381mobile element insertion1nstd203human GRCh38 chr11: 10,460,576-10,460,580 , GRCh37.p13 chr11: 10,482,123-10,482,127 AMPD3
    nsv5120085mobile element insertion1nstd203human GRCh38 chr11: 10,460,578-10,460,580 , GRCh37.p13 chr11: 10,482,125-10,482,127 AMPD3
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