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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
    nsv5038796inversion1nstd200human GRCh37.p13 chr7: 132,494,283-133,221,300 , GRCh38 chr7: 132,809,522-133,536,546 CHCHD3, EXOC4, 7 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4881561inversion1nstd200human GRCh37 chr7: 132,494,283-133,221,300 , GRCh38.p12 chr7: 132,809,522-133,536,546 CHCHD3, EXOC4, 7 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    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
    nsv4675687copy number variation1nstd102humanUncertain significance GRCh37 chr7: 131,443,245-133,276,729 , GRCh38.p12 chr7: 131,758,486-133,591,975 LOC105375512, ST13P7, 17 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
    nsv4675615copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620 ATG9B, OR10AC1, 603 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
    nsv4674926copy number variation1nstd102humanUncertain significance GRCh37 chr7: 130,604,326-133,333,388 , GRCh38.p12 chr7: 130,919,567-133,648,635 RPL31P36, LOC100506937, 29 more genes
    nsv4524360copy number variation1nstd166human GRCh37.p13 chr7: 132,496,866-132,877,221 , GRCh38.p12 chr7: 132,812,105-133,192,463 CHCHD3, ST13P7, 4 more genes
    nsv4455631copy number variation1nstd102humanUncertain significance GRCh37 chr7: 132,665,541-133,087,547 , GRCh38.p12 chr7: 132,980,781-133,402,793 EXOC4, CHCHD3, 7 more genes
    nsv4455493copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,592,554-159,119,707 , GRCh38.p12 chr7: 130,907,795-159,327,017 OR2A1, LOC101027084, 614 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
    nsv3924585copy number variation1nstd102humanPathogenic NCBI36 chr7: 130,506,777-158,812,468 , GRCh38 chr7: 131,171,478-159,327,017 , GRCh37 chr7: 130,856,237-159,119,707 PAXBP1P1, RNY3, 611 more genes
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