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Items: 1 to 20 of 170

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926454copy number variation1nstd209human GRCh38 chr7: 99,373,473-99,373,647 , GRCh37.p13 chr7: 98,971,096-98,971,270 ARPC1B
    nsv5915732copy number variation1nstd209human GRCh38 chr7: 99,219,897-99,375,922 , GRCh37.p13 chr7: 98,817,520-98,973,545 ARPC1B, ARPC1A, 3 more genes
    nsv5674024copy number variation2nstd102humanPathogenic GRCh37 chr7: 98,967,376-98,976,509 , GRCh38 chr7: 99,369,753-99,378,886 ARPC1B
    nsv5581916copy number variation1nstd207human GRCh38 chr7: 99,373,473-99,373,647 , GRCh37.p13 chr7: 98,971,096-98,971,270 ARPC1B
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5491998copy number variation1nstd206human GRCh38 chr7: 99,373,479-99,373,871 , GRCh37.p13 chr7: 98,971,102-98,971,494 ARPC1B
    nsv5388116copy number variation1nstd186human GRCh37 chr7: 98,971,154-98,971,361 , GRCh38.p12 chr7: 99,373,531-99,373,738 ARPC1B
    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
    nsv5321926inversion1nstd204human GRCh37.p13 chr7: 93,899,155-99,360,080 , GRCh38.p13 chr7: 94,269,843-99,762,457 , CYP3A51P, 118 more genes
    nsv5102077mobile element insertion1nstd203human GRCh38 chr7: 99,388,796-99,388,812 , GRCh37.p13 chr7: 98,986,419-98,986,435 ARPC1B
    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
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4819726copy number variation1nstd200human GRCh37 chr7: 98,990,517-98,990,889 , GRCh38.p12 chr7: 99,392,894-99,393,266 ARPC1B, PDAP1
    nsv4819725copy number variation1nstd200human GRCh37 chr7: 98,971,103-98,971,391 , GRCh38.p12 chr7: 99,373,480-99,373,768 ARPC1B
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4649298copy number variation1nstd186human GRCh37 chr7: 98,971,097-98,971,271 , GRCh38.p12 chr7: 99,373,474-99,373,648 ARPC1B
    nsv4637118copy number variation1nstd186human GRCh37 chr7: 98,971,102-98,971,299 , GRCh38.p12 chr7: 99,373,479-99,373,676 ARPC1B
    nsv4613856copy number variation1nstd183human GRCh37 chr7: 98,971,885-98,972,342 , GRCh38.p12 chr7: 99,374,262-99,374,719 ARPC1B
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