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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959764insertion1nstd209human GRCh37.p13 chr7: 27,179,620-27,179,620 , GRCh38 chr7: 27,140,001-27,140,001 HOXA3, HOXA5, 1 more genes
    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
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4828836copy number variation1nstd200human GRCh37 chr7: 27,075,050-27,459,025 , GRCh38.p12 chr7: 27,035,431-27,419,406 HOTAIRM1, HOXA-AS2, 24 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
    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
    nsv3970567insertion1nstd168human GRCh38 chr7: 27,135,064-27,148,375 , GRCh37.p13 chr7: 27,174,683-27,187,994 HOXA3, HOXA5, 2 more genes
    nsv3922885copy number variation1nstd102humanPathogenic GRCh38 chr7: 20,561,456-32,005,143 , GRCh37 chr7: 20,601,079-32,044,755 , NCBI36 chr7: 20,567,604-32,011,280 IL6-AS1, HOXA10-AS, 195 more genes
    nsv3922329copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-27,236,023 , GRCh38 chr7: 43,360-27,196,404 , NCBI36 chr7: 138,443-27,202,548 LOC401312, IQCE, 411 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3918785copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-37,129,317 , NCBI36 chr7: 149,268-37,095,842 , GRCh38 chr7: 54,185-37,089,712 MMD2, ICA1-AS1, 554 more genes
    nsv3916518copy number variation1nstd102humanPathogenic GRCh37 chr7: 1,737,760-27,246,914 , NCBI36 chr7: 1,704,286-27,213,439 , GRCh38 chr7: 1,698,124-27,207,295 LOC105375156, LOC105375133, 365 more genes
    nsv3916054copy number variation1nstd102humanPathogenic NCBI36 chr7: 20,217,060-27,855,544 , GRCh37 chr7: 20,250,535-27,889,019 , GRCh38 chr7: 20,210,912-27,849,400 MIR148A, NFE2L3, 139 more genes
    nsv3915802copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-41,915,483 , GRCh38 chr7: 54,185-41,875,885 , NCBI36 chr7: 149,268-41,882,008 RPL23AP52, IQCE, 638 more genes
    nsv3915436copy number variation1nstd102humanPathogenic NCBI36 chr7: 5,688,366-27,236,455 , GRCh37 chr7: 5,721,840-27,269,930 , GRCh38 chr7: 5,682,209-27,230,311 LOC101154643, SUMO2P14, 295 more genes
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