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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5944965copy number variation1nstd209human GRCh38 chr20: 453,228-454,100 , GRCh37.p13 chr20: 433,872-434,744 TBC1D20
    nsv5933936copy number variation1nstd209human GRCh38 chr20: 453,339-454,107 , GRCh37.p13 chr20: 433,983-434,751 TBC1D20
    nsv5708683mobile element insertion1nstd211human GRCh38 chr20: 449,305-449,305 , GRCh37.p13 chr20: 429,949-429,949 TBC1D20
    nsv5589894copy number variation1nstd207human GRCh38 chr20: 453,339-454,107 , GRCh37.p13 chr20: 433,983-434,751 TBC1D20
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5524491copy number variation1nstd206human GRCh38 chr20: 397,311-501,964 , GRCh37.p13 chr20: 377,955-482,608 CSNK2A1, TBC1D20, 2 more genes
    nsv5392572copy number variation1nstd186human GRCh37 chr20: 434,167-434,611 , GRCh38.p12 chr20: 453,523-453,967 TBC1D20
    nsv5391678copy number variation1nstd186human GRCh37 chr20: 433,909-434,400 , GRCh38.p12 chr20: 453,265-453,756 TBC1D20
    nsv5390196copy number variation1nstd186human GRCh37 chr20: 434,036-434,711 , GRCh38.p12 chr20: 453,392-454,067 TBC1D20
    nsv5381806copy number variation1nstd102humanPathogenic GRCh37 chr20: 67,778-974,841 , GRCh38.p12 chr20: 87,137-994,198 DEFB132, LOC101929937, 24 more genes
    nsv5328076copy number variation1nstd204human GRCh38.p13 chr20: 453,392-454,071 , GRCh37.p13 chr20: 434,036-434,715 TBC1D20
    nsv5299202copy number variation1nstd204human GRCh38.p13 chr20: 453,301-454,100 , GRCh37.p13 chr20: 433,945-434,744 TBC1D20
    nsv5160821mobile element insertion1nstd203human GRCh38 chr20: 447,195-447,209 , GRCh37.p13 chr20: 427,839-427,853 TBC1D20
    nsv5028306copy number variation1nstd200human GRCh38 chr20: 453,264-453,757 , GRCh37.p13 chr20: 433,908-434,401 TBC1D20
    nsv5028305copy number variation1nstd200human GRCh38 chr20: 453,521-453,968 , GRCh37.p13 chr20: 434,165-434,612 TBC1D20
    nsv5025038copy number variation1nstd200human GRCh38 chr20: 330,808-437,338 , GRCh37.p13 chr20: 311,452-417,982 TBC1D20, RBCK1, 3 more genes
    nsv4861591copy number variation1nstd200human GRCh37 chr20: 434,036-434,711 , GRCh38.p12 chr20: 453,392-454,067 TBC1D20
    nsv4768382copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 378,136-547,319 , GRCh38.p12 chr20: 397,492-566,675 CSNK2A1, RBCK1, 2 more genes
    nsv4729808copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,568-677,437 , GRCh38.p12 chr20: 80,927-696,793 CSNK2A1, SOX12, 18 more genes
    nsv4684288copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-813,880 , GRCh38.p12 chr20: 82,603-833,237 DEFB129, C20orf96, 20 more genes
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