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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5944078copy number variation1nstd209human GRCh38 chr18: 35,663,801-35,677,588 , GRCh37.p13 chr18: 33,243,765-33,257,552 LOC105372065, GALNT1
    nsv5936969copy number variation1nstd209human GRCh38 chr18: 35,687,182-35,689,167 , GRCh37.p13 chr18: 33,267,146-33,269,131 LOC105372064, GALNT1
    nsv5936816copy number variation1nstd209human GRCh38 chr18: 35,689,289-35,691,009 , GRCh37.p13 chr18: 33,269,253-33,270,973 GALNT1, LOC105372064
    nsv5930974copy number variation1nstd209human GRCh38 chr18: 35,654,800-35,663,625 , GRCh37.p13 chr18: 33,234,764-33,243,589 GALNT1
    nsv5930814copy number variation1nstd209human GRCh38 chr18: 35,683,595-35,687,011 , GRCh37.p13 chr18: 33,263,559-33,266,975 GALNT1
    nsv5929297copy number variation1nstd209human GRCh38 chr18: 35,702,992-35,703,504 , GRCh37.p13 chr18: 33,282,956-33,283,468 GALNT1, LOC105372064
    nsv5928634copy number variation1nstd209human GRCh38 chr18: 35,703,642-35,709,621 , GRCh37.p13 chr18: 33,283,606-33,289,585 LOC105372064, GALNT1
    nsv5927654copy number variation1nstd209human GRCh38 chr18: 35,677,755-35,683,387 , GRCh37.p13 chr18: 33,257,719-33,263,351 GALNT1, LOC105372065
    nsv5726943mobile element insertion1nstd211human GRCh38 chr18: 35,687,358-35,687,358 , GRCh37.p13 chr18: 33,267,322-33,267,322 GALNT1
    nsv5709598mobile element insertion1nstd211human GRCh38 chr18: 35,693,814-35,693,814 , GRCh37.p13 chr18: 33,273,778-33,273,778 LOC105372064, GALNT1
    nsv5702589mobile element insertion1nstd211human GRCh38 chr18: 35,675,019-35,675,019 , GRCh37.p13 chr18: 33,254,983-33,254,983 GALNT1, LOC105372065
    nsv5560879mobile element insertion1nstd206human GRCh38 chr18: 35,687,358-35,687,409 , GRCh37.p13 chr18: 33,267,322-33,267,373 GALNT1
    nsv5532030copy number variation1nstd206human GRCh38 chr18: 35,678,306-35,679,595 , GRCh37.p13 chr18: 33,258,270-33,259,559 GALNT1
    nsv5429940mobile element insertion1nstd206human GRCh38 chr18: 35,693,814-35,693,859 , GRCh37.p13 chr18: 33,273,778-33,273,823 GALNT1, LOC105372064
    nsv5366483translocation1nstd200human GRCh38 chr2: 122,697,579-122,697,579 , GRCh38 chr18: 35,709,961-35,709,961 , GRCh37.p13 chr2: 123,455,155-123,455,155 , GRCh37.p13 chr18: 33,289,925-33,289,925 GALNT1, LOC105372064
    nsv5336584translocation1nstd200human GRCh37 chr18: 33,289,925-33,289,925 , GRCh37 chr2: 123,455,155-123,455,155 , GRCh38.p12 chr2: 122,697,579-122,697,579 , GRCh38.p12 chr18: 35,709,961-35,709,961 GALNT1, LOC105372064
    nsv5187783mobile element insertion1nstd203human GRCh38 chr18: 35,678,506-35,678,521 , GRCh37.p13 chr18: 33,258,470-33,258,485 GALNT1
    nsv5156056mobile element insertion1nstd203human GRCh38 chr18: 35,670,677-35,670,692 , GRCh37.p13 chr18: 33,250,641-33,250,656 GALNT1, LOC105372065
    nsv5145273mobile element insertion1nstd203human GRCh38 chr18: 35,669,733-35,669,747 , GRCh37.p13 chr18: 33,249,697-33,249,711 GALNT1, LOC105372065
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