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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919512copy number variation1nstd209human GRCh38 chr7: 26,509,679-33,120,288 , GRCh37.p13 chr7: 26,549,298-33,159,900 , CPVL-AS1, 126 more genes
    nsv5914132copy number variation1nstd209human GRCh38 chr7: 26,936,027-36,716,695 , GRCh37.p13 chr7: 26,975,646-36,756,300 , HOXA7, 162 more genes
    nsv5846918copy number variation1nstd209human GRCh38 chr7: 29,649,777-29,702,809 , GRCh37.p13 chr7: 29,689,393-29,742,425 ZNRF2P2, LOC646762, 2 more genes
    nsv5846289copy number variation2nstd209human GRCh38 chr7: 29,677,029-29,682,161 , GRCh37.p13 chr7: 29,716,645-29,721,777 MIR550A3, LOC646762
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5555679sequence alteration1nstd206human GRCh38 chr7: 29,674,660-30,295,579 , GRCh37.p13 chr7: 29,714,276-30,335,195 RPS27P16, ZNRF2P2, 15 more genes
    nsv5489248copy number variation1nstd206human GRCh38 chr7: 29,632,621-29,746,242 , GRCh37.p13 chr7: 29,672,237-29,785,858 , LOC646762, 3 more genes
    nsv5487005copy number variation1nstd206human GRCh38 chr7: 28,971,005-29,835,164 , GRCh37.p13 chr7: 29,010,621-29,874,780 , ZNRF2P2, 15 more genes
    nsv5483908copy number variation1nstd206human GRCh38 chr7: 29,640,242-29,748,350 , GRCh37.p13 chr7: 29,679,858-29,787,966 , ZNRF2P2, 3 more genes
    nsv5239820copy number variation1nstd204human GRCh38.p13 chr7: 29,680,798-29,695,987 , GRCh37.p13 chr7: 29,720,414-29,735,603 MIR550A3, DPY19L2P3, 2 more genes
    nsv5225931copy number variation1nstd204human GRCh38.p13 chr7: 29,650,177-29,694,028 , GRCh37.p13 chr7: 29,689,793-29,733,644 MIR550A3, LOC646762, 2 more genes
    nsv5225250copy number variation1nstd204human GRCh38.p13 chr7: 29,633,301-29,684,400 , GRCh37.p13 chr7: 29,672,917-29,724,016 , DPY19L2P3, 3 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956193copy number variation1nstd200human GRCh38 chr7: 29,665,067-29,701,257 , GRCh37.p13 chr7: 29,704,683-29,740,873 ZNRF2P2, LOC646762, 2 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4811198copy number variation1nstd200human GRCh37 chr7: 29,704,683-29,740,873 , GRCh38.p12 chr7: 29,665,067-29,701,257 ZNRF2P2, LOC646762, 2 more genes
    nsv4675863copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 28,487,175-32,037,495 , GRCh38.p12 chr7: 28,447,557-31,997,883 ADCYAP1R1, AQP1, 55 more genes
    nsv4674822copy number variation1nstd102humanPathogenic GRCh37 chr7: 23,877,135-33,139,446 , GRCh38.p12 chr7: 23,837,516-33,099,834 RP9P, LINC00997, 156 more genes
    nsv4605219copy number variation2nstd183human GRCh37 chr7: 29,671,940-29,767,315 , GRCh38.p12 chr7: 29,632,324-29,727,699 , ZNRF2P2, 3 more genes
    nsv4603791copy number variation2nstd183human GRCh37 chr7: 29,672,462-29,788,198 , GRCh38.p12 chr7: 29,632,846-29,748,582 , DPY19L2P3, 3 more genes
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