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Items: 1 to 20 of 149

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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
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5488967copy number variation1nstd206human GRCh38 chr7: 100,362,019-100,384,064 , GRCh37.p13 chr7: 99,959,642-99,981,687 PILRA, PILRB, 1 more genes
    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
    nsv5370857translocation1nstd200human GRCh38 chr7: 100,382,410-100,382,410 , GRCh38 chr7: 100,382,358-100,382,358 , GRCh37.p13 chr7: 99,979,981-99,979,981 , GRCh37.p13 chr7: 99,980,033-99,980,033 PILRA
    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
    nsv5183089mobile element insertion1nstd203human GRCh38 chr7: 100,388,088-100,388,103 , GRCh37.p13 chr7: 99,985,711-99,985,726 PILRA
    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
    nsv4965034copy number variation1nstd200human GRCh38 chr7: 100,379,646-100,380,422 , GRCh37.p13 chr7: 99,977,269-99,978,045 PILRA
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4819755copy number variation1nstd200human GRCh37 chr7: 99,975,338-99,975,858 , GRCh38.p12 chr7: 100,377,715-100,378,235 PILRA
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4729729copy number variation1nstd102humanLikely benign GRCh37 chr7: 99,901,525-100,004,543 , GRCh38.p12 chr7: 100,303,902-100,406,920 PMS2P1, PILRB, 7 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
    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
    nsv4171987copy number variation1nstd166human GRCh37.p13 chr7: 99,979,981-99,980,033 , GRCh38.p12 chr7: 100,382,358-100,382,410 PILRA
    nsv4164822copy number variation1nstd166human GRCh37.p13 chr7: 99,964,000-99,973,250 , GRCh38.p12 chr7: 100,366,377-100,375,627 PILRA, PILRB, 1 more genes
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