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Items: 1 to 20 of 162

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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
    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
    nsv5335708translocation1nstd200human GRCh37 chr7: 99,307,985-99,307,985 , GRCh37 chr7: 99,306,881-99,306,881 , GRCh38.p12 chr7: 99,710,362-99,710,362 , GRCh38.p12 chr7: 99,709,258-99,709,258 CYP3A7, ZSCAN25, 1 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
    nsv5321926inversion1nstd204human GRCh37.p13 chr7: 93,899,155-99,360,080 , GRCh38.p13 chr7: 94,269,843-99,762,457 , CYP3A51P, 118 more genes
    nsv5103637mobile element insertion1nstd203human GRCh38 chr7: 99,729,082-99,729,098 , GRCh37.p13 chr7: 99,326,705-99,326,721 CYP3A7, ZSCAN25, 1 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
    nsv4966671copy number variation1nstd200human GRCh38 chr7: 99,715,811-99,720,266 , GRCh37.p13 chr7: 99,313,434-99,317,889 CYP3A7, ZSCAN25, 1 more genes
    nsv4966670copy number variation1nstd200human GRCh38 chr7: 99,694,767-99,695,614 , GRCh37.p13 chr7: 99,292,390-99,293,237 ZSCAN25, CYP3A7-CYP3A51P, 1 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4708246copy number variation1nstd195human GRCh37 chr7: 99,257,651-99,283,701 , GRCh38.p12 chr7: 99,660,028-99,686,078 CYP3A5, CYP3A51P, 2 more genes
    nsv4706950copy number variation1nstd195human GRCh37 chr7: 99,290,101-99,342,251 , GRCh38.p12 chr7: 99,692,478-99,744,628 CYP3A7, CYP3A51P, 2 more genes
    nsv4602504copy number variation1nstd183human GRCh37 chr7: 99,322,829-99,327,194 , GRCh38.p12 chr7: 99,725,206-99,729,571 ZSCAN25, CYP3A7, 1 more genes
    nsv4490434mobile element insertion1nstd166human GRCh37.p13 chr7: 99,312,668-99,312,668 , GRCh38.p12 chr7: 99,715,045-99,715,045 CYP3A7, ZSCAN25, 1 more genes
    nsv4455239copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,758,955-99,368,262 , GRCh38.p12 chr7: 99,161,332-99,770,639 TMEM225B, CYP3A7-CYP3A51P, 28 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
    nsv4164769copy number variation1nstd166human GRCh37.p13 chr7: 99,297,000-99,349,000 , GRCh38.p12 chr7: 99,699,377-99,751,377 CYP3A7-CYP3A51P, CYP3A51P, 3 more genes
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