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Items: 1 to 20 of 95

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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
    nsv5381783copy number variation1nstd102humanPathogenic GRCh37 chr7: 41,124,364-47,945,566 , GRCh38.p12 chr7: 41,084,766-47,905,969 ELK1P1, URGCP, 121 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956381copy number variation1nstd200human GRCh38 chr7: 42,905,412-42,908,318 , GRCh37.p13 chr7: 42,945,011-42,947,917 C7orf25
    nsv4953626copy number variation1nstd200human GRCh38 chr7: 42,376,110-43,620,617 , GRCh37.p13 chr7: 42,415,709-43,660,216 TCP1P1, LOC105375250, 19 more genes
    nsv4811471copy number variation1nstd200human GRCh37 chr7: 42,945,011-42,947,917 , GRCh38.p12 chr7: 42,905,412-42,908,318 C7orf25
    nsv4456214copy number variation2nstd102humanUncertain significance GRCh37 chr7: 42,417,642-43,658,492 , GRCh38.p12 chr7: 42,378,043-43,618,893 RPL18AP10, LOC105375252, 19 more genes
    nsv4455566copy number variation1nstd102humanUncertain significance GRCh37 chr7: 42,421,780-43,664,397 , GRCh38.p12 chr7: 42,382,181-43,624,798 RNU7-35P, LINC01448, 19 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
    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
    nsv3924656copy number variation1nstd102humanUncertain significance GRCh38 chr7: 42,452,844-43,608,265 , GRCh37 chr7: 42,492,443-43,647,864 , NCBI36 chr7: 42,458,968-43,614,389 LINC01448, MIR3943, 19 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
    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
    nsv3917401copy number variation1nstd102humanPathogenic GRCh38 chr7: 42,388,724-43,606,751 , NCBI36 chr7: 42,394,848-43,612,875 , GRCh37 chr7: 42,428,323-43,646,350 MIR3943, LINC01448, 19 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
    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
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