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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125911copy number variation1nstd186human GRCh37 chr19: 58,658,805-58,659,158 , GRCh38.p12 chr19: 58,147,438-58,147,791 ZNF329
    nsv5604279copy number variation1nstd207human GRCh38 chr19: 58,147,434-58,147,735 , GRCh37.p13 chr19: 58,658,801-58,659,102 ZNF329
    nsv5533101copy number variation1nstd206human GRCh38 chr19: 58,136,606-58,136,880 , GRCh37.p13 chr19: 58,647,973-58,648,247 ZNF329
    nsv5528779copy number variation1nstd206human GRCh38 chr19: 58,140,525-58,140,854 , GRCh37.p13 chr19: 58,651,892-58,652,221 ZNF329
    nsv5521112copy number variation1nstd206human GRCh38 chr19: 58,149,466-58,150,467 , GRCh37.p13 chr19: 58,660,833-58,661,834 ZNF329
    nsv5516751copy number variation1nstd206human GRCh38 chr19: 58,147,438-58,147,791 , GRCh37.p13 chr19: 58,658,805-58,659,158 ZNF329
    nsv5323230copy number variation1nstd204human GRCh38.p13 chr19: 58,144,261-58,145,361 , GRCh37.p13 chr19: 58,655,628-58,656,728 ZNF329
    nsv5280745copy number variation1nstd204human GRCh38.p13 chr19: 57,881,401-58,501,600 , GRCh37.p13 chr19: 58,392,769-59,012,967 ZNF417, LOC112268251, 51 more genes
    nsv5025027copy number variation1nstd200human GRCh38 chr19: 58,130,565-58,167,729 , GRCh37.p13 chr19: 58,641,932-58,679,096 ZNF329
    nsv5025025copy number variation1nstd200human GRCh38 chr19: 58,101,230-58,193,466 , GRCh37.p13 chr19: 58,612,597-58,704,833 ZSCAN18, ZNF329, 1 more genes
    nsv5025024copy number variation1nstd200human GRCh38 chr19: 58,091,835-58,168,844 , GRCh37.p13 chr19: 58,603,202-58,680,211 ZSCAN18, ZNF329
    nsv4865386copy number variation1nstd200human GRCh37 chr19: 58,612,597-58,704,833 , GRCh38.p12 chr19: 58,101,230-58,193,466 ZNF329, ZNF274, 1 more genes
    nsv4861528copy number variation1nstd200human GRCh37 chr19: 58,664,693-58,665,537 , GRCh38.p12 chr19: 58,153,326-58,154,170 ZNF329
    nsv4738572copy number variation1nstd199human GRCh37 chr19: 58,658,904-58,659,002 , GRCh38.p12 chr19: 58,147,537-58,147,635 ZNF329
    nsv4712183translocation1nstd195human GRCh37 chr7: 54,734,867-54,734,867 , GRCh37 chr19: 58,659,583-58,659,583 , GRCh38.p12 chr19: 58,148,216-58,148,216 , GRCh38.p12 chr7: 54,667,174-54,667,174 ZNF329
    nsv4710699translocation1nstd195human GRCh37 chr7: 54,734,868-54,734,868 , GRCh37 chr19: 58,659,583-58,659,583 , GRCh38.p12 chr19: 58,148,216-58,148,216 , GRCh38.p12 chr7: 54,667,175-54,667,175 ZNF329
    nsv4676227copy number variation1nstd102humanUncertain significance GRCh37 chr19: 58,647,621-58,703,491 , GRCh38.p12 chr19: 58,136,254-58,192,124 ZNF329, ZNF274
    nsv4632108copy number variation1nstd183human GRCh37 chr19: 58,580,277-58,828,076 , GRCh38.p12 chr19: 58,068,909-58,316,710 ZNF329, ZSCAN18, 12 more genes
    nsv4537697copy number variation1nstd166human GRCh37.p13 chr19: 58,658,829-58,658,902 , GRCh38.p12 chr19: 58,147,462-58,147,535 ZNF329
    nsv4457732copy number variation1nstd102humanUncertain significance GRCh37 chr19: 57,952,073-58,661,581 , GRCh38.p12 chr19: 57,440,705-58,150,214 ZNF418, ZNF606-AS1, 39 more genes
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