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Items: 1 to 20 of 241

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5937790copy number variation1nstd209human GRCh38 chr17: 30,668,045-32,084,125 , GRCh37.p13 chr17: 28,995,063-30,411,144 , OMG, 39 more genes
    nsv5673111copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,587,625-29,669,475 , GRCh38.p12 chr17: 31,260,607-31,342,457 NF1, LOC101927057, 3 more genes
    nsv5673110copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,586,040-29,701,173 , GRCh38.p12 chr17: 31,259,022-31,374,155 AK4P1, EVI2A, 4 more genes
    nsv5673107copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,527,428-29,657,848 , GRCh38.p12 chr17: 31,200,410-31,330,830 EVI2A, NF1, 3 more genes
    nsv5673103copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,422,322-29,664,606 , GRCh38.p12 chr17: 31,095,304-31,337,588 EVI2A, EVI2B, 3 more genes
    nsv5673033copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,587,381-29,662,055 , GRCh38.p12 chr17: 31,260,363-31,335,037 EVI2B, OMG, 3 more genes
    nsv5673031copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,422,322-29,701,178 , GRCh38.p12 chr17: 31,095,304-31,374,160 AK4P1, EVI2A, 4 more genes
    nsv5672966copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,588,709-29,701,193 , GRCh38.p12 chr17: 31,261,691-31,374,175 AK4P1, EVI2A, 4 more genes
    nsv5672965copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,559,081-29,701,173 , GRCh38.p12 chr17: 31,232,063-31,374,155 AK4P1, EVI2A, 4 more genes
    nsv5672961copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,422,322-29,665,163 , GRCh38.p12 chr17: 31,095,304-31,338,145 NF1, LOC101927057, 3 more genes
    nsv5672960copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr17: 29,422,055-29,701,173 , GRCh38.p12 chr17: 31,095,037-31,374,155 AK4P1, EVI2A, 4 more genes
    nsv5672874copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,592,237-29,653,280 , GRCh38.p12 chr17: 31,265,219-31,326,262 NF1, LOC101927057, 3 more genes
    nsv5544481insertion1nstd206human GRCh38 chr17: 31,312,227-31,312,270 , GRCh37.p13 chr17: 29,639,245-29,639,288 NF1, EVI2B
    nsv5381008copy number variation1nstd102humanUncertain significance GRCh37 chr17: 29,622,128-29,701,173 , GRCh38.p12 chr17: 31,295,110-31,374,155 OMG, EVI2A, 3 more genes
    nsv5187104mobile element insertion1nstd203human GRCh38 chr17: 31,302,162-31,302,179 , GRCh37.p13 chr17: 29,629,180-29,629,197 EVI2B, NF1
    nsv5154303mobile element insertion1nstd203human GRCh38 chr17: 31,312,213-31,312,227 , GRCh37.p13 chr17: 29,639,231-29,639,245 NF1, EVI2B
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729791copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,039,844-30,412,788 , GRCh38.p12 chr17: 30,712,826-32,085,769 ADAP2, TEFM, 37 more genes
    nsv4684241copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,393,104-30,427,403 , GRCh38.p12 chr17: 31,066,086-32,100,384 LOC102724625, RNA5SP437, 26 more genes
    nsv4683828copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 29,575,992-29,679,442 , GRCh38.p12 chr17: 31,248,974-31,352,424 AK4P1, EVI2A, 4 more genes
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