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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960909insertion1nstd209human GRCh38 chr7: 95,371,278-95,371,278 , GRCh37.p13 chr7: 95,000,590-95,000,590 PON3
    nsv5925127copy number variation1nstd209human GRCh38 chr7: 95,384,344-95,388,079 , GRCh37.p13 chr7: 95,013,656-95,017,391 PON3
    nsv5687294mobile element insertion2nstd211human GRCh38 chr7: 95,363,616-95,363,616 , GRCh37.p13 chr7: 94,992,928-94,992,928 PON3
    nsv5638370insertion1nstd207human GRCh38 chr7: 95,371,278-95,371,278 , GRCh37.p13 chr7: 95,000,590-95,000,590 PON3
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5489129copy number variation1nstd206human GRCh38 chr7: 95,368,684-95,374,506 , GRCh37.p13 chr7: 94,997,996-95,003,818 PON3
    nsv5407295mobile element insertion1nstd206human GRCh38 chr7: 95,363,607-95,363,607 , GRCh37.p13 chr7: 94,992,919-94,992,919 PON3
    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
    nsv5321926inversion1nstd204human GRCh37.p13 chr7: 93,899,155-99,360,080 , GRCh38.p13 chr7: 94,269,843-99,762,457 , CYP3A51P, 118 more genes
    nsv5197940mobile element insertion1nstd203human GRCh38 chr7: 95,371,282-95,371,290 , GRCh37.p13 chr7: 95,000,594-95,000,602 PON3
    nsv5194836mobile element insertion1nstd203human GRCh38 chr7: 95,371,280-95,371,290 , GRCh37.p13 chr7: 95,000,592-95,000,602 PON3
    nsv5188151mobile element insertion1nstd203human GRCh38 chr7: 95,371,278-95,371,289 , GRCh37.p13 chr7: 95,000,590-95,000,601 PON3
    nsv5187159mobile element insertion1nstd203human GRCh38 chr7: 95,371,283-95,371,289 , GRCh37.p13 chr7: 95,000,595-95,000,601 PON3
    nsv5183410mobile element insertion1nstd203human GRCh38 chr7: 95,371,277-95,371,290 , GRCh37.p13 chr7: 95,000,589-95,000,602 PON3
    nsv5182863mobile element insertion1nstd203human GRCh38 chr7: 95,371,281-95,371,289 , GRCh37.p13 chr7: 95,000,593-95,000,601 PON3
    nsv5114002mobile element insertion1nstd203human GRCh38 chr7: 95,363,604-95,363,616 , GRCh37.p13 chr7: 94,992,916-94,992,928 PON3
    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
    nsv4957740copy number variation1nstd200human GRCh38 chr7: 95,390,655-95,390,784 , GRCh37.p13 chr7: 95,019,967-95,020,096 PON3
    nsv4957739copy number variation1nstd200human GRCh38 chr7: 95,368,684-95,374,506 , GRCh37.p13 chr7: 94,997,996-95,003,818 PON3
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