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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5893458copy number variation1nstd209human GRCh38 chr2: 231,451,279-231,451,577 , GRCh37.p13 chr2: 232,315,990-232,316,288 NCL
    nsv5689974mobile element insertion2nstd211human GRCh38 chr2: 231,457,410-231,457,410 , GRCh37.p13 chr2: 232,322,121-232,322,121 NCL
    nsv5571584copy number variation1nstd207human GRCh38 chr2: 231,464,731-231,465,285 , GRCh37.p13 chr2: 232,329,442-232,329,996 NCL
    nsv5438677copy number variation1nstd206human GRCh38 chr2: 231,464,731-231,465,289 , GRCh37.p13 chr2: 232,329,442-232,330,000 NCL
    nsv5408216mobile element insertion1nstd206human GRCh38 chr2: 231,457,410-231,457,461 , GRCh37.p13 chr2: 232,322,121-232,322,172 NCL
    nsv5351196translocation1nstd200human GRCh38 chr2: 231,461,858-231,461,858 , GRCh38 chr2: 231,461,916-231,461,916 , GRCh37.p13 chr2: 232,326,569-232,326,569 , GRCh37.p13 chr2: 232,326,627-232,326,627 NCL
    nsv5344135translocation1nstd200human GRCh37 chr2: 232,326,627-232,326,627 , GRCh37 chr2: 232,326,569-232,326,569 , GRCh38.p12 chr2: 231,461,858-231,461,858 , GRCh38.p12 chr2: 231,461,916-231,461,916 NCL
    nsv5205400copy number variation1nstd204human GRCh38.p13 chr2: 231,458,072-231,459,071 , GRCh37.p13 chr2: 232,322,783-232,323,782 NCL, SNORD82
    nsv5075968mobile element insertion1nstd203human GRCh38 chr2: 231,457,396-231,457,408 , GRCh37.p13 chr2: 232,322,107-232,322,119 NCL
    nsv5074319mobile element insertion1nstd203human GRCh38 chr2: 231,457,400-231,457,410 , GRCh37.p13 chr2: 232,322,111-232,322,121 NCL
    nsv5068747mobile element insertion1nstd203human GRCh38 chr2: 231,457,394-231,457,410 , GRCh37.p13 chr2: 232,322,105-232,322,121 NCL
    nsv5063346mobile element insertion1nstd203human GRCh38 chr2: 231,457,403-231,457,410 , GRCh37.p13 chr2: 232,322,114-232,322,121 NCL
    nsv4914036copy number variation1nstd200human GRCh38 chr2: 231,444,784-231,451,577 , GRCh37.p13 chr2: 232,309,495-232,316,288 NCL
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4720679insertion1nstd186human GRCh37 chr2: 232,322,107-232,322,107 , GRCh38.p12 chr2: 231,457,396-231,457,396 NCL
    nsv4673913copy number variation1nstd102humanPathogenic GRCh37 chr2: 230,814,690-242,783,384 , GRCh38.p12 chr2: 229,949,974-241,841,232 MIR2467, D2HGDH, 270 more genes
    nsv4585505copy number variation1nstd183human GRCh37 chr2: 232,327,474-232,327,911 , GRCh38.p12 chr2: 231,462,763-231,463,200 NCL
    nsv4583437copy number variation1nstd183human GRCh37 chr2: 232,327,474-232,329,333 , GRCh38.p12 chr2: 231,462,763-231,464,622 NCL
    nsv4544774insertion1nstd166human GRCh37.p13 chr2: 232,322,107-232,322,107 , GRCh38.p12 chr2: 231,457,396-231,457,396 NCL
    nsv4435891copy number variation1nstd102humanPathogenic GRCh37 chr2: 210,779,657-239,879,183 , GRCh38.p12 chr2: 209,914,933-238,957,487 XRCC5, LINC01173, 494 more genes
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