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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950584insertion1nstd209human GRCh38 chr7: 30,968,640-30,968,640 , GRCh37.p13 chr7: 31,008,255-31,008,255 GHRHR
    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
    nsv5627321insertion1nstd207human GRCh38 chr7: 30,968,640-30,968,640 , GRCh37.p13 chr7: 31,008,255-31,008,255 GHRHR
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5543631insertion1nstd206human GRCh38 chr7: 30,968,602-30,968,640 , GRCh37.p13 chr7: 31,008,217-31,008,255 GHRHR
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4953552copy number variation1nstd200human GRCh38 chr7: 30,612,963-31,127,528 , GRCh37.p13 chr7: 30,652,579-31,167,142 , INMT-MINDY4, 12 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
    nsv4680029copy number variation1nstd189human GRCh37.p13 chr7: 30,820,895-31,201,645 , GRCh38.p12 chr7: 30,781,279-31,162,031 , ADCYAP1R1, 8 more genes
    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
    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
    nsv4397170copy number variation1nstd174human GRCh37 chr7: 30,649,212-31,185,096 , GRCh38.p12 chr7: 30,609,596-31,145,482 , CRHR2, 13 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
    nsv4142758copy number variation1nstd166human GRCh37.p13 chr7: 31,011,234-31,011,713 , GRCh38.p12 chr7: 30,971,619-30,972,098 GHRHR
    nsv3950517insertion1nstd167human GRCh37 chr7: 31,008,255-31,008,255 , GRCh38.p12 chr7: 30,968,640-30,968,640 GHRHR
    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
    nsv3922530copy number variation1nstd102humanUncertain significance GRCh38 chr7: 30,621,519-31,115,117 , GRCh37 chr7: 30,661,135-31,154,731 , NCBI36 chr7: 30,627,660-31,121,256 ADCYAP1R1, INMT-MINDY4, 11 more genes
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