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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922472copy number variation1nstd209human GRCh38 chr7: 30,008,447-30,008,702 , GRCh37.p13 chr7: 30,048,063-30,048,318 FKBP14-AS1, FKBP14
    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
    nsv5567958copy number variation1nstd207human GRCh38 chr7: 30,011,535-30,011,596 , GRCh37.p13 chr7: 30,051,151-30,051,212 FKBP14, FKBP14-AS1
    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
    nsv5482634copy number variation1nstd206human GRCh38 chr7: 30,008,660-30,009,914 , GRCh37.p13 chr7: 30,048,276-30,049,530 FKBP14-AS1, FKBP14
    nsv5381467copy number variation1nstd102humanUncertain significance GRCh37 chr7: 30,049,199-30,067,417 , GRCh38.p12 chr7: 30,009,583-30,027,801 FKBP14, PLEKHA8, 1 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4953545copy number variation1nstd200human GRCh38 chr7: 29,725,651-30,417,635 , GRCh37.p13 chr7: 29,765,267-30,457,251 LINC01176, WIPF3, 14 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4729079copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 29,758,030-31,318,843 , GRCh38.p12 chr7: 29,718,414-31,279,229 ADCYAP1R1, AQP1, 33 more genes
    nsv4683534copy number variation1nstd102humanUncertain significance GRCh37 chr7: 30,050,189-30,054,519 , GRCh38.p12 chr7: 30,010,573-30,014,903 FKBP14, FKBP14-AS1
    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
    nsv4674951copy number variation1nstd102humanUncertain significance GRCh37 chr7: 29,803,827-30,071,557 , GRCh38.p12 chr7: 29,764,211-30,031,941 WIPF3, FKBP14, 3 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
    nsv4523933copy number variation1nstd166human GRCh37.p13 chr7: 30,050,837-30,050,969 , GRCh38.p12 chr7: 30,011,221-30,011,353 FKBP14, FKBP14-AS1
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4435897copy number variation1nstd102humanPathogenic GRCh37 chr7: 23,236,782-30,690,453 , GRCh38.p12 chr7: 23,197,163-30,650,837 CCDC126, LOC389473, 138 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
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