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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933689copy number variation1nstd209human GRCh38 chr17: 34,993,209-34,994,147 , GRCh37.p13 chr17: 33,320,228-33,321,166 LIG3
    nsv5886611copy number variation1nstd209human GRCh38 chr17: 34,993,201-34,994,200 , GRCh37.p13 chr17: 33,320,220-33,321,219 LIG3
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5522880copy number variation1nstd206human GRCh38 chr17: 34,993,212-34,994,148 , GRCh37.p13 chr17: 33,320,231-33,321,167 LIG3
    nsv5358827translocation1nstd200human GRCh38 chr17: 34,994,148-34,994,148 , GRCh38 chr17: 34,993,212-34,993,212 , GRCh37.p13 chr17: 33,320,231-33,320,231 , GRCh37.p13 chr17: 33,321,167-33,321,167 LIG3
    nsv5320668copy number variation1nstd204human GRCh38.p13 chr17: 34,993,208-34,994,149 , GRCh37.p13 chr17: 33,320,227-33,321,168 LIG3
    nsv5157471mobile element insertion1nstd203human GRCh38 chr17: 34,978,690-34,978,739 , GRCh37.p13 chr17: 33,305,709-33,305,758 LIG3, CCT6B
    nsv5148019mobile element insertion1nstd203human GRCh38 chr17: 35,002,498-35,002,498 , GRCh37.p13 chr17: 33,329,517-33,329,517 LIG3
    nsv5029046copy number variation1nstd200human GRCh38 chr17: 34,959,348-34,982,808 , GRCh37.p13 chr17: 33,286,367-33,309,827 ZNF830, LIG3, 1 more genes
    nsv5016124copy number variation1nstd200human GRCh38 chr17: 34,998,910-34,999,752 , GRCh37.p13 chr17: 33,325,929-33,326,771 LIG3
    nsv4858653copy number variation1nstd200human GRCh37 chr17: 33,320,231-33,321,167 , GRCh38.p12 chr17: 34,993,212-34,994,148 LIG3
    nsv4858652copy number variation1nstd200human GRCh37 chr17: 33,304,834-33,306,763 , GRCh38.p12 chr17: 34,977,815-34,979,744 CCT6B, LIG3
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4675860copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,073,917-33,863,479 , GRCh38.p12 chr17: 34,746,898-35,536,460 RPL37P22, LIG3, 26 more genes
    nsv4629346copy number variation1nstd183human GRCh37 chr17: 33,319,139-33,339,863 , GRCh38.p12 chr17: 34,992,120-35,012,844 OSTCP7, RAD51L3-RFFL, 2 more genes
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4436271copy number variation1nstd102humanUncertain significance GRCh37 chr17: 31,889,285-33,557,612 , GRCh38.p12 chr17: 33,562,266-35,230,593 LOC105371739, CCL7, 33 more genes
    nsv4384972copy number variation1nstd173human GRCh37 chr17: 27,710,978-33,392,085 , GRCh38.p12 chr17: 29,383,960-35,065,066 , LOC105371737, 137 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4242145copy number variation1nstd166human GRCh37.p13 chr17: 33,332,929-33,333,891 , GRCh38.p12 chr17: 35,005,910-35,006,872 RFFL, LIG3, 1 more genes
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