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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960250insertion1nstd209human GRCh38 chr7: 113,909,427-113,909,427 , GRCh37.p13 chr7: 113,549,482-113,549,482 PPP1R3A
    nsv5910900copy number variation1nstd209human GRCh38 chr7: 113,890,302-113,890,389 , GRCh37.p13 chr7: 113,530,357-113,530,444 PPP1R3A
    nsv5686669mobile element insertion1nstd211human GRCh38 chr7: 113,881,418-113,881,418 , GRCh37.p13 chr7: 113,521,473-113,521,473 PPP1R3A
    nsv5678711mobile element insertion1nstd211human GRCh38 chr7: 113,878,219-113,878,219 , GRCh37.p13 chr7: 113,518,274-113,518,274 PPP1R3A
    nsv5678576mobile element insertion2nstd211human GRCh38 chr7: 113,909,444-113,909,444 , GRCh37.p13 chr7: 113,549,499-113,549,499 PPP1R3A
    nsv5637003insertion1nstd207human GRCh38 chr7: 113,909,427-113,909,427 , GRCh37.p13 chr7: 113,549,482-113,549,482 PPP1R3A
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5413821mobile element insertion1nstd206human GRCh38 chr7: 113,878,219-113,878,270 , GRCh37.p13 chr7: 113,518,274-113,518,325 PPP1R3A
    nsv5406690mobile element insertion1nstd206human GRCh38 chr7: 113,881,418-113,881,469 , GRCh37.p13 chr7: 113,521,473-113,521,524 PPP1R3A
    nsv5400276mobile element insertion1nstd206human GRCh38 chr7: 113,909,427-113,909,427 , GRCh37.p13 chr7: 113,549,482-113,549,482 PPP1R3A
    nsv5371024translocation1nstd200human GRCh38 chr7: 113,897,091-113,897,091 , GRCh38 chr7: 113,897,144-113,897,144 , GRCh37.p13 chr7: 113,537,199-113,537,199 , GRCh37.p13 chr7: 113,537,146-113,537,146 PPP1R3A
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5180269mobile element insertion1nstd203human GRCh38 chr7: 113,883,982-113,883,986 , GRCh37.p13 chr7: 113,524,037-113,524,041 PPP1R3A
    nsv5119733mobile element insertion1nstd203human GRCh38 chr7: 113,909,427-113,909,444 , GRCh37.p13 chr7: 113,549,482-113,549,499 PPP1R3A
    nsv5103944mobile element insertion1nstd203human GRCh38 chr7: 113,888,858-113,888,866 , GRCh37.p13 chr7: 113,528,913-113,528,921 PPP1R3A
    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
    nsv4951056copy number variation1nstd200human GRCh38 chr7: 113,917,521-113,918,546 , GRCh37.p13 chr7: 113,557,576-113,558,601 PPP1R3A
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4743244copy number variation1nstd199human GRCh37 chr7: 113,525,719-113,525,783 , GRCh38.p12 chr7: 113,885,664-113,885,728 PPP1R3A
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