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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918110copy number variation1nstd209human GRCh38 chr7: 130,674,280-130,676,999 , GRCh37.p13 chr7|NW_003871065.1: 353,511-356,230 , GRCh37.p13 chr7: 130,359,120-130,361,839 TSGA13
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5489260copy number variation1nstd206human GRCh38 chr7: 130,674,240-130,677,056 , GRCh37.p13 chr7|NW_003871065.1: 353,471-356,287 , GRCh37.p13 chr7: 130,359,080-130,361,896 TSGA13
    nsv5476059copy number variation1nstd206human GRCh38 chr7: 130,679,152-130,679,249 , GRCh37.p13 chr7: 130,363,990-130,364,087 , GRCh37.p13 chr7|NW_003871065.1: 358,383-358,480 TSGA13
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5111660mobile element insertion1nstd203human GRCh38 chr7: 130,673,695-130,673,717 , GRCh37.p13 chr7|NW_003871065.1: 352,926-352,948 , GRCh37.p13 chr7: 130,358,535-130,358,557 TSGA13
    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
    nsv4958337copy number variation1nstd200human GRCh38 chr7: 130,678,339-130,680,407 , GRCh37.p13 chr7|NW_003871065.1: 357,570-359,638 , GRCh37.p13 chr7: 130,363,179-130,365,245 TSGA13
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4825341copy number variation1nstd200human GRCh37 chr7: 130,359,100-130,361,897 , GRCh38.p12 chr7: 130,674,260-130,677,057 TSGA13
    nsv4820570copy number variation1nstd200human GRCh37 chr7: 130,363,179-130,365,245 , GRCh38.p12 chr7: 130,678,339-130,680,407 TSGA13
    nsv4820569copy number variation1nstd200human GRCh37 chr7: 130,351,836-130,352,242 , GRCh38.p12 chr7: 130,666,996-130,667,402 COPG2, TSGA13
    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
    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
    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
    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
    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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