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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904586copy number variation1nstd209human GRCh38 chr2: 233,739,757-233,751,413 , GRCh37.p13 chr2: 234,648,403-234,660,059 UGT1A10, UGT1A6, 9 more genes
    nsv5902563copy number variation1nstd209human GRCh38 chr2: 233,743,844-233,755,120 , GRCh37.p13 chr2: 234,652,490-234,663,766 UGT1A6, UGT1A10, 10 more genes
    nsv5892353copy number variation1nstd209human GRCh38 chr2: 233,725,506-233,743,754 , GRCh37.p13 chr2: 234,634,152-234,652,400 UGT1A, UGT1A6, 8 more genes
    nsv5832813copy number variation2nstd209human GRCh38 chr2: 233,739,656-233,744,566 , GRCh37.p13 chr2: 234,648,302-234,653,212 UGT1A4, UGT1A7, 8 more genes
    nsv5832791copy number variation2nstd209human GRCh38 chr2: 233,743,524-233,752,090 , GRCh37.p13 chr2: 234,652,170-234,660,736 UGT1A9, UGT1A, 9 more genes
    nsv5832551copy number variation2nstd209human GRCh38 chr2: 233,743,523-233,748,500 , GRCh37.p13 chr2: 234,652,169-234,657,146 UGT1A8, UGT1A3, 9 more genes
    nsv5568587copy number variation1nstd207human GRCh38 chr2: 233,739,805-233,751,461 , GRCh37.p13 chr2: 234,648,451-234,660,107 UGT1A7, UGT1A4, 9 more genes
    nsv5384995copy number variation1nstd186human GRCh37 chr2: 234,648,459-234,660,012 , GRCh38.p12 chr2: 233,739,813-233,751,366 UGT1A4, UGT1A2P, 9 more genes
    nsv5383197copy number variation1nstd186human GRCh37 chr2: 234,648,460-234,660,011 , GRCh38.p12 chr2: 233,739,814-233,751,365 UGT1A8, UGT1A5, 9 more genes
    nsv4926765copy number variation1nstd200human GRCh38 chr2: 233,739,813-233,751,367 , GRCh37.p13 chr2: 234,648,459-234,660,013 UGT1A8, UGT1A4, 9 more genes
    nsv4806333copy number variation1nstd200human GRCh37 chr2: 234,648,457-234,660,014 , GRCh38.p12 chr2: 233,739,811-233,751,368 UGT1A10, UGT1A6, 9 more genes
    nsv4768328copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,110,452-243,028,452 , GRCh38.p12 chr2: 232,245,742-242,086,301 LOC107985836, LOC105373980, 217 more genes
    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
    nsv4674274copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,090,049-239,494,702 , GRCh38.p12 chr2: 233,181,403-238,586,061 LOC105373933, CEP19P1, 105 more genes
    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
    nsv4664582copy number variation1nstd186human GRCh37 chr2: 234,648,159-234,659,534 , GRCh38.p12 chr2: 233,739,513-233,750,888 UGT1A3, UGT1A4, 9 more genes
    nsv4658847copy number variation1nstd186human GRCh37 chr2: 234,648,505-234,661,581 , GRCh38.p12 chr2: 233,739,859-233,752,935 UGT1A6, LOC100286922, 10 more genes
    nsv4655903copy number variation1nstd186human GRCh37 chr2: 234,648,371-234,660,038 , GRCh38.p12 chr2: 233,739,725-233,751,392 UGT1A10, UGT1A6, 9 more genes
    nsv4595402copy number variation1nstd183human GRCh37 chr2: 234,648,505-234,661,581 , GRCh38.p12 chr2: 233,739,859-233,752,935 UGT1A4, UGT1A10, 10 more genes
    nsv4583237copy number variation1nstd183human GRCh37 chr2: 234,648,265-234,659,429 , GRCh38.p12 chr2: 233,739,619-233,750,783 UGT1A4, UGT1A, 9 more genes
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