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Items: 1 to 20 of 269

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128902copy number variation1nstd186human GRCh37 chr22: 46,690,159-46,690,492 , GRCh38.p12 chr22: 46,294,262-46,294,595 GTSE1, TTC38, 1 more genes
    nsv5977305insertion1nstd209human GRCh38 chr22: 46,290,586-46,290,586 , GRCh37.p13 chr22: 46,686,483-46,686,483 TTC38
    nsv5955587copy number variation1nstd209human GRCh38 chr22: 46,287,073-46,290,164 , GRCh37.p13 chr22: 46,682,970-46,686,061 TTC38
    nsv5952614copy number variation1nstd209human GRCh38 chr22: 46,294,262-46,294,593 , GRCh37.p13 chr22: 46,690,159-46,690,490 GTSE1, TTC38, 1 more genes
    nsv5950120copy number variation1nstd209human GRCh38 chr22: 46,290,477-46,290,649 , GRCh37.p13 chr22: 46,686,374-46,686,546 TTC38
    nsv5880193copy number variation2nstd209human GRCh38 chr22: 46,289,119-46,290,318 , GRCh37.p13 chr22: 46,685,016-46,686,215 TTC38
    nsv5871124copy number variation1nstd209human GRCh38 chr22: 46,287,069-46,290,268 , GRCh37.p13 chr22: 46,682,966-46,686,165 TTC38
    nsv5670137insertion1nstd207human GRCh38 chr22: 46,290,466-46,290,466 , GRCh37.p13 chr22: 46,686,363-46,686,363 TTC38
    nsv5666494insertion1nstd207human GRCh38 chr22: 46,276,717-46,276,717 , GRCh37.p13 chr22: 46,672,614-46,672,614 TTC38
    nsv5601984copy number variation1nstd207human GRCh38 chr22: 46,294,251-46,294,582 , GRCh37.p13 chr22: 46,690,148-46,690,479 GTSE1, TTC38, 1 more genes
    nsv5594083copy number variation1nstd207human GRCh38 chr22: 46,290,482-46,290,652 , GRCh37.p13 chr22: 46,686,379-46,686,549 TTC38
    nsv5550253copy number variation1nstd206human GRCh38 chr22: 46,290,155-46,290,819 , GRCh37.p13 chr22: 46,686,052-46,686,716 TTC38
    nsv5537636copy number variation1nstd206human GRCh38 chr22: 46,294,262-46,294,595 , GRCh37.p13 chr22: 46,690,159-46,690,492 GTSE1, GTSE1-DT, 1 more genes
    nsv5391579copy number variation1nstd186human GRCh37 chr22: 46,690,219-46,690,492 , GRCh38.p12 chr22: 46,294,322-46,294,595 GTSE1, TTC38, 1 more genes
    nsv5381149copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,333,802-51,195,728 , GRCh38.p12 chr22: 41,937,798-50,757,300 WBP2NL, RN7SKP80, 210 more genes
    nsv5282808copy number variation1nstd204human GRCh38.p13 chr22: 46,294,301-46,294,600 , GRCh37.p13 chr22: 46,690,198-46,690,497 GTSE1-DT, GTSE1, 1 more genes
    nsv5034276copy number variation1nstd200human GRCh38 chr22: 46,290,155-46,290,819 , GRCh37.p13 chr22: 46,686,052-46,686,716 TTC38
    nsv5033697copy number variation1nstd200human GRCh38 chr22: 46,278,467-46,278,610 , GRCh37.p13 chr22: 46,674,364-46,674,507 TTC38
    nsv5032814copy number variation1nstd200human GRCh38 chr22: 46,266,177-46,420,843 , GRCh37.p13 chr22: 46,662,074-46,816,740 TRMU, TTC38, 3 more genes
    nsv4886474copy number variation1nstd200human GRCh37 chr22: 46,690,217-46,690,493 , GRCh38.p12 chr22: 46,294,320-46,294,596 TTC38, GTSE1-DT, 1 more genes
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