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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5699770mobile element insertion1nstd211human GRCh38 chr11: 111,402,327-111,402,327 , GRCh37.p13 chr11: 111,273,052-111,273,052 BTG4
    nsv5695025mobile element insertion1nstd211human GRCh38 chr11: 111,401,081-111,401,081 , GRCh37.p13 chr11: 111,271,806-111,271,806 BTG4
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5660907insertion1nstd207human GRCh38 chr11: 111,423,300-111,423,300 , GRCh37.p13 chr11: 111,294,025-111,294,025 BTG4
    nsv5646011insertion1nstd207human GRCh38 chr11: 111,429,926-111,429,926 , GRCh37.p13 chr11: 111,300,651-111,300,651 BTG4
    nsv5513060copy number variation1nstd206human GRCh38 chr11: 111,485,174-111,485,227 , GRCh37.p13 chr11: 111,355,899-111,355,952 BTG4
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    nsv5497137copy number variation1nstd206human GRCh38 chr11: 111,503,318-111,503,416 , GRCh37.p13 chr11: 111,374,043-111,374,141 BTG4
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5339221translocation1nstd200human GRCh37 chr11: 111,355,952-111,355,952 , GRCh37 chr11: 111,355,899-111,355,899 , GRCh38.p12 chr11: 111,485,174-111,485,174 , GRCh38.p12 chr11: 111,485,227-111,485,227 BTG4
    nsv5135501mobile element insertion1nstd203human GRCh38 chr11: 111,402,312-111,402,327 , GRCh37.p13 chr11: 111,273,037-111,273,052 BTG4
    nsv5133156mobile element insertion1nstd203human GRCh38 chr11: 111,382,691-111,382,704 , GRCh37.p13 chr11: 111,253,416-111,253,429 BTG4, RNU2-60P
    nsv5128302mobile element insertion1nstd203human GRCh38 chr11: 111,394,958-111,394,969 , GRCh37.p13 chr11: 111,265,683-111,265,694 BTG4
    nsv4989298copy number variation1nstd200human GRCh38 chr11: 111,496,095-111,534,266 , GRCh37.p13 chr11: 111,366,820-111,404,991 BTG4, MIR34C, 3 more genes
    nsv4980672copy number variation1nstd200human GRCh38 chr11: 111,502,146-111,507,380 , GRCh37.p13 chr11: 111,372,871-111,378,105 BTG4
    nsv4980671copy number variation1nstd200human GRCh38 chr11: 111,494,694-111,507,408 , GRCh37.p13 chr11: 111,365,419-111,378,133 BTG4
    nsv4980670copy number variation1nstd200human GRCh38 chr11: 111,494,725-111,502,002 , GRCh37.p13 chr11: 111,365,450-111,372,727 BTG4
    nsv4980669copy number variation1nstd200human GRCh38 chr11: 111,489,178-111,493,091 , GRCh37.p13 chr11: 111,359,903-111,363,816 BTG4
    nsv4980668copy number variation1nstd200human GRCh38 chr11: 111,408,556-111,410,199 , GRCh37.p13 chr11: 111,279,281-111,280,924 BTG4
    nsv4847656copy number variation1nstd200human GRCh37 chr11: 111,365,419-111,378,132 , GRCh38.p12 chr11: 111,494,694-111,507,407 BTG4
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