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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121004copy number variation1nstd186human GRCh37 chr16: 55,841,912-55,865,212 , GRCh38.p12 chr16: 55,808,000-55,831,300 CES1
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5979417inversion1nstd209human GRCh38 chr16: 55,828,618-55,892,245 , GRCh37.p13 chr16: 55,862,530-55,926,157 CES1, CES5A
    nsv5975759inversion1nstd209human GRCh38 chr16: 55,762,863-55,830,847 , GRCh37.p13 chr16: 55,796,775-55,864,759 CES1, CES1P1
    nsv5881121copy number variation1nstd209human GRCh38 chr16: 55,824,027-55,831,164 , GRCh37.p13 chr16: 55,857,939-55,865,076 CES1
    nsv5875564copy number variation1nstd209human GRCh38 chr16: 55,810,655-55,828,624 , GRCh37.p13 chr16: 55,844,567-55,862,536 CES1
    nsv5873165copy number variation1nstd209human GRCh38 chr16: 55,806,596-55,819,478 , GRCh37.p13 chr16: 55,840,508-55,853,390 CES1
    nsv5665020inversion1nstd207human GRCh38 chr16: 55,798,353-55,831,288 , GRCh37.p13 chr16: 55,832,265-55,865,200 CES1
    nsv5659104insertion1nstd207human GRCh38 chr16: 55,820,003-55,820,003 , GRCh37.p13 chr16: 55,853,915-55,853,915 CES1
    nsv5646641insertion1nstd207human GRCh38 chr16: 55,817,047-55,817,047 , GRCh37.p13 chr16: 55,850,959-55,850,959 CES1
    nsv5645806insertion1nstd207human GRCh38 chr16: 55,830,781-55,830,781 , GRCh37.p13 chr16: 55,864,693-55,864,693 CES1
    nsv5563138inversion1nstd206human GRCh38 chr16: 55,759,814-55,833,953 , GRCh37.p13 chr16: 55,793,726-55,867,865 CES1, CES1P1
    nsv5559483sequence alteration1nstd206human GRCh38 chr16: 55,760,567-55,833,083 , GRCh37.p13 chr16: 55,794,479-55,866,995 CES1, CES1P1
    nsv5557619sequence alteration1nstd206human GRCh38 chr16: 55,728,286-55,826,123 , GRCh37.p13 chr16: 55,762,198-55,860,035 CES1, CES1P1, 1 more genes
    nsv5531811copy number variation1nstd206human GRCh38 chr16: 55,808,000-55,831,300 , GRCh37.p13 chr16: 55,841,912-55,865,212 CES1
    nsv5313898copy number variation1nstd204human GRCh38.p13 chr16: 55,765,916-55,812,550 , GRCh37.p13 chr16: 55,799,828-55,846,462 CES1P1, CES1
    nsv5278898copy number variation1nstd204human GRCh38.p13 chr16: 55,807,001-55,833,500 , GRCh37.p13 chr16: 55,840,913-55,867,412 CES1
    nsv5277779copy number variation1nstd204human GRCh38.p13 chr16: 55,821,701-55,824,400 , GRCh37.p13 chr16: 55,855,613-55,858,312 CES1
    nsv5277016copy number variation1nstd204human GRCh38.p13 chr16: 55,808,301-55,816,600 , GRCh37.p13 chr16: 55,842,213-55,850,512 CES1
    nsv5276793copy number variation1nstd204human GRCh38.p13 chr16: 55,806,701-55,820,900 , GRCh37.p13 chr16: 55,840,613-55,854,812 CES1
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