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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979182inversion1nstd209human GRCh38 chr7: 99,981,419-101,289,122 , GRCh37.p13 chr7: 99,579,042-100,932,403 , ACHE, 92 more genes
    nsv5923434copy number variation1nstd209human GRCh38 chr7: 100,668,951-100,672,861 , GRCh37.p13 chr7: 100,266,574-100,270,484 GNB2
    nsv5863877copy number variation1nstd209human GRCh38 chr7: 100,668,984-100,672,913 , GRCh37.p13 chr7: 100,266,607-100,270,536 GNB2
    nsv5857524copy number variation2nstd209human GRCh38 chr7: 100,671,153-100,672,613 , GRCh37.p13 chr7: 100,268,776-100,270,236 GNB2
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5556207sequence alteration1nstd206human GRCh38 chr7: 100,499,061-100,696,513 , GRCh37.p13 chr7: 100,096,684-100,294,136 TFR2, IRS3P, 13 more genes
    nsv5477348copy number variation1nstd206human GRCh38 chr7: 100,668,960-100,672,862 , GRCh37.p13 chr7: 100,266,583-100,270,485 GNB2
    nsv5476553copy number variation1nstd206human GRCh38 chr7: 100,674,973-100,675,551 , GRCh37.p13 chr7: 100,272,596-100,273,174 GNB2
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 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
    nsv5259343copy number variation1nstd204human GRCh38.p13 chr7: 100,051,301-100,949,000 , GRCh37.p13 chr7: 99,648,924-100,546,632 , MEPCE, 70 more genes
    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
    nsv4966712copy number variation1nstd200human GRCh38 chr7: 100,669,038-100,672,856 , GRCh37.p13 chr7: 100,266,661-100,270,479 GNB2
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4819763copy number variation1nstd200human GRCh37 chr7: 100,266,667-100,270,559 , GRCh38.p12 chr7: 100,669,044-100,672,936 GNB2
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4710370copy number variation1nstd195human GRCh37 chr7: 100,122,201-100,327,551 , GRCh38.p12 chr7: 100,524,578-100,729,928 , POP7, 15 more genes
    nsv4684274copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 99,593,346-102,470,275 , GRCh38.p12 chr7: 99,995,723-102,829,828 ACHE, AP1S1, 124 more genes
    nsv4658842copy number variation1nstd186human GRCh37 chr7: 100,270,701-100,274,100 , GRCh38.p12 chr7: 100,673,078-100,676,477 GNB2
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