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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5866371copy number variation1nstd209human GRCh38 chr12: 55,388,402-55,390,501 , GRCh37.p13 chr12: 55,782,186-55,784,285 OR6C66P
    nsv5722061mobile element insertion2nstd211human GRCh38 chr12: 55,388,454-55,388,454 , GRCh37.p13 chr12: 55,782,238-55,782,238 OR6C66P
    nsv5653383insertion1nstd207human GRCh38 chr12: 55,388,439-55,388,439 , GRCh37.p13 chr12: 55,782,223-55,782,223 OR6C66P
    nsv5562083mobile element insertion1nstd206human GRCh38 chr12: 55,388,454-55,388,505 , GRCh37.p13 chr12: 55,782,238-55,782,289 OR6C66P
    nsv5555472mobile element insertion1nstd206human GRCh38 chr12: 55,388,389-55,388,439 , GRCh37.p13 chr12: 55,782,173-55,782,223 OR6C66P
    nsv5279162copy number variation1nstd204human GRCh38.p13 chr12: 55,388,401-55,392,400 , GRCh37.p13 chr12: 55,782,185-55,786,184 OR6C66P
    nsv5269573copy number variation1nstd204human GRCh38.p13 chr12: 55,388,302-55,390,401 , GRCh37.p13 chr12: 55,782,086-55,784,185 OR6C66P
    nsv5268808copy number variation1nstd204human GRCh38.p13 chr12: 55,386,119-55,391,201 , GRCh37.p13 chr12: 55,779,903-55,784,985 OR6C66P
    nsv5262968copy number variation1nstd204human GRCh38.p13 chr12: 55,388,601-55,395,000 , GRCh37.p13 chr12: 55,782,385-55,788,784 OR6C66P, OR6C73P
    nsv5199937mobile element insertion1nstd203human GRCh38 chr12: 55,388,440-55,388,440 , GRCh37.p13 chr12: 55,782,224-55,782,224 OR6C66P
    nsv5197905mobile element insertion1nstd203human GRCh38 chr12: 55,388,443-55,388,443 , GRCh37.p13 chr12: 55,782,227-55,782,227 OR6C66P
    nsv5194561mobile element insertion1nstd203human GRCh38 chr12: 55,388,446-55,388,446 , GRCh37.p13 chr12: 55,782,230-55,782,230 OR6C66P
    nsv5193629mobile element insertion1nstd203human GRCh38 chr12: 55,388,445-55,388,445 , GRCh37.p13 chr12: 55,782,229-55,782,229 OR6C66P
    nsv5191592mobile element insertion1nstd203human GRCh38 chr12: 55,388,439-55,388,439 , GRCh37.p13 chr12: 55,782,223-55,782,223 OR6C66P
    nsv5191343mobile element insertion1nstd203human GRCh38 chr12: 55,388,442-55,388,442 , GRCh37.p13 chr12: 55,782,226-55,782,226 OR6C66P
    nsv5189911mobile element insertion1nstd203human GRCh38 chr12: 55,388,433-55,388,433 , GRCh37.p13 chr12: 55,782,217-55,782,217 OR6C66P
    nsv5187223mobile element insertion1nstd203human GRCh38 chr12: 55,388,441-55,388,441 , GRCh37.p13 chr12: 55,782,225-55,782,225 OR6C66P
    nsv5187103mobile element insertion1nstd203human GRCh38 chr12: 55,388,444-55,388,444 , GRCh37.p13 chr12: 55,782,228-55,782,228 OR6C66P
    nsv5184170mobile element insertion1nstd203human GRCh38 chr12: 55,388,434-55,388,442 , GRCh37.p13 chr12: 55,782,218-55,782,226 OR6C66P
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
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