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Items: 1 to 20 of 1115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5948343insertion1nstd209human GRCh38 chr6: 151,736,375-151,736,375 , GRCh37.p13 chr6: 152,057,510-152,057,510 ESR1
    nsv5907377copy number variation1nstd209human GRCh38 chr6: 151,732,238-151,739,480 , GRCh37.p13 chr6: 152,053,373-152,060,615 ESR1
    nsv5907320copy number variation1nstd209human GRCh38 chr6: 151,982,534-151,990,636 , GRCh37.p13 chr6: 152,303,669-152,311,771 ESR1
    nsv5905905copy number variation1nstd209human GRCh38 chr6: 151,920,620-151,921,599 , GRCh37.p13 chr6: 152,241,755-152,242,734 ESR1
    nsv5898231copy number variation1nstd209human GRCh38 chr6: 151,779,805-151,779,921 , GRCh37.p13 chr6: 152,100,940-152,101,056 ESR1
    nsv5897048copy number variation1nstd209human GRCh38 chr6: 152,050,391-152,052,028 , GRCh37.p13 chr6: 152,371,526-152,373,163 ESR1
    nsv5896941copy number variation1nstd209human GRCh38 chr6: 152,068,854-152,071,097 , GRCh37.p13 chr6: 152,389,989-152,392,232 ESR1
    nsv5896515copy number variation1nstd209human GRCh38 chr6: 152,103,954-152,104,101 , GRCh37.p13 chr6: 152,425,089-152,425,236 ESR1
    nsv5895743copy number variation1nstd209human GRCh38 chr6: 151,751,774-151,751,980 , GRCh37.p13 chr6: 152,072,909-152,073,115 ESR1
    nsv5892816copy number variation1nstd209human GRCh38 chr6: 152,081,300-152,081,741 , GRCh37.p13 chr6: 152,402,435-152,402,876 ESR1
    nsv5891249copy number variation1nstd209human GRCh38 chr6: 151,818,956-151,821,940 , GRCh37.p13 chr6: 152,140,091-152,143,075 ESR1
    nsv5844755copy number variation1nstd209human GRCh38 chr6: 152,068,905-152,071,104 , GRCh37.p13 chr6: 152,390,040-152,392,239 ESR1
    nsv5844668copy number variation2nstd209human GRCh38 chr6: 151,984,215-151,986,645 , GRCh37.p13 chr6: 152,305,350-152,307,780 ESR1
    nsv5844667copy number variation1nstd209human GRCh38 chr6: 151,982,415-151,990,622 , GRCh37.p13 chr6: 152,303,550-152,311,757 ESR1
    nsv5844666copy number variation1nstd209human GRCh38 chr6: 151,732,224-151,739,481 , GRCh37.p13 chr6: 152,053,359-152,060,616 ESR1
    nsv5844130copy number variation1nstd209human GRCh38 chr6: 152,050,368-152,051,962 , GRCh37.p13 chr6: 152,371,503-152,373,097 ESR1
    nsv5844129copy number variation1nstd209human GRCh38 chr6: 151,824,727-151,825,926 , GRCh37.p13 chr6: 152,145,862-152,147,061 ESR1
    nsv5844087copy number variation1nstd209human GRCh38 chr6: 151,818,959-151,821,758 , GRCh37.p13 chr6: 152,140,094-152,142,893 ESR1
    nsv5718733mobile element insertion2nstd211human GRCh38 chr6: 152,039,476-152,039,476 , GRCh37.p13 chr6: 152,360,611-152,360,611 ESR1
    nsv5691602mobile element insertion1nstd211human GRCh38 chr6: 151,850,125-151,850,125 , GRCh37.p13 chr6: 152,171,260-152,171,260 ESR1
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