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Items: 1 to 20 of 94

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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
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4966337copy number variation1nstd200human GRCh38 chr7: 40,507,175-40,595,638 , GRCh37.p13 chr7: 40,546,774-40,635,237 SUGCT-AS1, LOC105375244, 1 more genes
    nsv4455279copy number variation1nstd102humanUncertain significance GRCh37 chr7: 40,198,215-43,252,984 , GRCh38.p12 chr7: 40,158,616-43,213,385 INHBA, LOC105375244, 34 more genes
    nsv4455211copy number variation1nstd102humanUncertain significance GRCh37 chr7: 40,081,970-40,611,718 , GRCh38.p12 chr7: 40,042,371-40,572,119 CDK13, MPLKIP, 6 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
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv3924742copy number variation1nstd102humanPathogenic GRCh37 chr7: 38,217,601-45,343,699 , GRCh38 chr7: 38,177,999-45,304,100 , NCBI36 chr7: 38,184,126-45,310,224 NUDCD3, KRT8P20, 152 more genes
    nsv3924054copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,573,756-56,174,815 , NCBI36 chr7: 40,540,281-56,142,309 , GRCh38 chr7: 40,534,157-56,107,122 VOPP1-DT, SGO1P2, 229 more genes
    nsv3921332copy number variation1nstd102humanUncertain significance NCBI36 chr7: 39,676,871-40,877,460 , GRCh37 chr7: 39,710,346-40,910,935 , GRCh38 chr7: 39,670,747-40,871,336 LOC112267984, RALA, 19 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
    nsv3918948copy number variation1nstd102humanPathogenic GRCh37 chr7: 39,103,000-45,402,695 , GRCh38 chr7: 39,063,400-45,363,096 , NCBI36 chr7: 39,069,525-45,369,220 MRPS23P1, CDK13, 120 more genes
    nsv3917263copy number variation1nstd102humanPathogenic GRCh38 chr7: 33,328,312-62,377,476 , GRCh37 chr7: 33,367,924-61,831,899 , NCBI36 chr7: 33,334,449-61,469,334 MIR4649, LOC107986794, 444 more genes
    nsv3916442copy number variation1nstd102humanPathogenic NCBI36 chr7: 37,309,607-48,670,880 , GRCh37 chr7: 37,343,082-48,700,334 , GRCh38 chr7: 37,303,478-48,660,738 LOC102724903, LINC01448, 204 more genes
    nsv3916363copy number variation1nstd102humanUncertain significance GRCh38 chr7: 39,251,052-40,641,073 , NCBI36 chr7: 39,257,176-40,647,197 , GRCh37 chr7: 39,290,651-40,680,672 MPLKIP, RNU6-719P, 27 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
    nsv3915283copy number variation1nstd102humanPathogenic GRCh37 chr7: 39,853,758-45,789,334 , GRCh38 chr7: 39,814,159-45,749,735 , NCBI36 chr7: 39,820,283-45,755,859 TUBG1P, CAMK2B, 108 more genes
    nsv3912277copy number variation1nstd102humanPathogenic NCBI36 chr7: 32,684,528-41,051,106 , GRCh37 chr7: 32,718,003-41,084,581 , GRCh38 chr7: 32,678,391-41,044,983 MATCAP2, LOC107986785, 134 more genes
    nsv3912038copy number variation1nstd102humanPathogenic GRCh38 chr7: 35,460,776-42,013,800 , NCBI36 chr7: 35,466,911-42,019,924 , GRCh37 chr7: 35,500,386-42,053,399 INHBA-AS1, LOC107986789, 110 more genes
    nsv3911166copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,060,197-50,611,198 , NCBI36 chr7: 40,026,722-50,578,692 , GRCh38 chr7: 40,020,598-50,543,500 SUGCT, C7orf57, 155 more genes
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