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Items: 1 to 20 of 228

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976174insertion1nstd209human GRCh38 chr14: 100,371,447-100,371,447 , GRCh37.p13 chr14: 100,837,784-100,837,784 WARS1
    nsv5695702mobile element insertion1nstd211human GRCh38 chr14: 100,332,634-100,332,634 , GRCh37.p13 chr14: 100,798,971-100,798,971 WARS1
    nsv5653722insertion1nstd207human GRCh38 chr14: 100,345,064-100,345,064 , GRCh37.p13 chr14: 100,811,401-100,811,401 WARS1
    nsv5510164copy number variation1nstd206human GRCh38 chr14: 100,357,562-100,357,615 , GRCh37.p13 chr14: 100,823,899-100,823,952 WARS1
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5428513mobile element insertion1nstd206human GRCh38 chr14: 100,332,634-100,332,685 , GRCh37.p13 chr14: 100,798,971-100,799,022 WARS1
    nsv5004994copy number variation1nstd200human GRCh38 chr14: 100,314,274-100,351,771 , GRCh37.p13 chr14: 100,780,611-100,818,108 WARS1, RN7SL523P, 1 more genes
    nsv5004992copy number variation1nstd200human GRCh38 chr14: 100,278,056-100,446,082 , GRCh37.p13 chr14: 100,744,393-100,912,419 WARS1, NDUFB3P4, 7 more genes
    nsv4991373copy number variation1nstd200human GRCh38 chr14: 100,354,722-100,358,973 , GRCh37.p13 chr14: 100,821,059-100,825,310 WARS1
    nsv4863597copy number variation1nstd200human GRCh37 chr14: 100,780,611-100,818,108 , GRCh38.p12 chr14: 100,314,274-100,351,771 RN7SL523P, WARS1, 1 more genes
    nsv4863596copy number variation1nstd200human GRCh37 chr14: 100,744,393-100,912,419 , GRCh38.p12 chr14: 100,278,056-100,446,082 MIR345, LOC105370664, 7 more genes
    nsv4765742insertion1nstd199human GRCh37 chr14: 100,811,295-100,811,295 , GRCh38.p12 chr14: 100,344,958-100,344,958 WARS1
    nsv4684265copy number variation1nstd102humanPathogenic GRCh37 chr14: 96,829,290-107,287,663 , GRCh38.p12 chr14: 96,362,953-106,879,456 NDUFB3P4, LINC02320, 502 more genes
    nsv4675243copy number variation1nstd102humanPathogenic GRCh37 chr14: 100,317,190-101,012,999 , GRCh38.p12 chr14: 99,850,853-100,546,662 RN7SKP92, MIR345, 20 more genes
    nsv4625194copy number variation1nstd183human GRCh37 chr14: 100,841,478-100,843,074 , GRCh38.p12 chr14: 100,375,141-100,376,737 WARS1, WDR25
    nsv4456178copy number variation1nstd102humanPathogenic GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229 LOC105370639, SERPINA9, 600 more genes
    nsv4455196copy number variation1nstd102humanUncertain significance GRCh37 chr14: 100,744,400-100,910,248 , GRCh38.p12 chr14: 100,278,063-100,443,911 SLC25A29, WARS1, 7 more genes
    nsv4455156copy number variation1nstd102humanPathogenic GRCh37 chr14: 99,794,230-107,285,437 , GRCh38.p12 chr14: 99,327,893-106,877,229 IGHG4, IGHV3-57, 464 more genes
    nsv4445696insertion1nstd175human GRCh37 chr14: 100,811,401-100,811,401 , GRCh38.p12 chr14: 100,345,064-100,345,064 WARS1
    nsv4349898copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 99,737,888-101,847,855 , GRCh38.p12 chr14: 99,271,551-101,381,518 EML1, WARS1, 136 more genes
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