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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4968766copy number variation1nstd200human GRCh38 chr7: 130,726,795-130,740,860 , GRCh37.p13 chr7|NW_003871065.1: 406,026-420,091 , GRCh37.p13 chr7: 130,411,622-130,425,621 KLF14, LOC105375508
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4756384insertion1nstd199human GRCh37 chr7: 130,418,880-130,418,880 , GRCh38.p12 chr7: 130,734,053-130,734,053 KLF14, LOC105375508
    nsv4729643copy number variation1nstd102humanUncertain significance GRCh37 chr7: 129,605,827-133,093,756 , GRCh38.p12 chr7: 129,965,987-133,409,002 LOC100506937, CPA1, 57 more genes
    nsv4721692insertion1nstd186human GRCh37 chr7: 130,418,883-130,418,883 , GRCh38.p12 chr7: 130,734,056-130,734,056 KLF14, LOC105375508
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4675089copy number variation1nstd102humanUncertain significance GRCh37 chr7: 129,997,717-133,355,098 , GRCh38.p12 chr7: 130,357,876-133,670,345 RPS14P10, PLXNA4, 48 more genes
    nsv4614911copy number variation1nstd183human GRCh37 chr7: 130,408,380-130,429,186 , GRCh38.p12 chr7: 130,723,552-130,744,427 KLF14, LOC105375508
    nsv4614717copy number variation1nstd183human GRCh37 chr7: 130,405,508-130,467,575 , GRCh38.p12 chr7: 130,720,680-130,782,816 LOC105375508, KLF14
    nsv4551260insertion1nstd166human GRCh37.p13 chr7: 130,418,883-130,418,883 , GRCh38.p12 chr7: 130,734,056-130,734,056 LOC105375508, KLF14
    nsv4456503copy number variation1nstd102humanUncertain significance GRCh37 chr7: 130,032,531-130,590,540 , GRCh38.p12 chr7: 130,392,690-130,905,781 LOC105375509, MESTIT1, 15 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
    nsv4446991insertion1nstd175human GRCh37 chr7: 130,418,883-130,418,883 , GRCh38.p12 chr7: 130,734,056-130,734,056 KLF14, LOC105375508
    nsv4436127complex substitution1nstd102humanLikely pathogenic GRCh37 chr7: 129,367,205-140,482,957 , GRCh38.p12 chr7: 129,727,365-140,783,157 AKR1B1, BPGM, 187 more genes
    nsv4405458copy number variation1nstd174human GRCh37 chr7: 130,407,589-130,469,097 , GRCh38.p12 chr7: 130,722,761-130,784,338 KLF14, LOC105375508
    nsv4349183copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,312,450-159,119,220 , GRCh38.p12 chr7: 128,672,396-159,326,530 LOC105375582, TRBJ2-4, 686 more genes
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