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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5944110copy number variation1nstd209human GRCh38 chr17: 47,304,855-47,306,926 , GRCh37.p13 chr17: 45,382,221-45,384,292 EFCAB13-DT, ITGB3
    nsv5878189copy number variation1nstd209human GRCh38 chr17: 47,304,845-47,306,986 , GRCh37.p13 chr17: 45,382,211-45,384,352 ITGB3, EFCAB13-DT
    nsv5697688mobile element insertion2nstd211human GRCh38 chr17: 47,261,439-47,261,439 , GRCh37.p13 chr17: 45,338,805-45,338,805 ITGB3
    nsv5654932insertion1nstd207human GRCh38 chr17: 47,261,424-47,261,424 , GRCh37.p13 chr17: 45,338,790-45,338,790 ITGB3
    nsv5563774sequence alteration1nstd206human GRCh38 chr17: 47,271,940-47,287,769 , GRCh37.p13 chr17: 45,349,306-45,365,135 ITGB3, LOC107985029
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5524064copy number variation1nstd206human GRCh38 chr17: 47,304,896-47,306,927 , GRCh37.p13 chr17: 45,382,262-45,384,293 ITGB3, EFCAB13-DT
    nsv5430610mobile element insertion1nstd206human GRCh38 chr17: 47,261,439-47,261,490 , GRCh37.p13 chr17: 45,338,805-45,338,856 ITGB3
    nsv5155005mobile element insertion1nstd203human GRCh38 chr17: 47,252,061-47,252,079 , GRCh37.p13 chr17: 45,329,427-45,329,445 ITGB3
    nsv5153734mobile element insertion1nstd203human GRCh38 chr17: 47,261,424-47,261,439 , GRCh37.p13 chr17: 45,338,790-45,338,805 ITGB3
    nsv5026282copy number variation1nstd200human GRCh38 chr17: 47,304,892-47,306,868 , GRCh37.p13 chr17: 45,382,258-45,384,234 ITGB3, EFCAB13-DT
    nsv5026281copy number variation1nstd200human GRCh38 chr17: 47,269,574-47,273,683 , GRCh37.p13 chr17: 45,346,940-45,351,049 ITGB3
    nsv4867175copy number variation1nstd200human GRCh37 chr17: 45,382,231-45,384,260 , GRCh38.p12 chr17: 47,304,865-47,306,894 ITGB3, EFCAB13-DT
    nsv4867174copy number variation1nstd200human GRCh37 chr17: 45,332,644-45,333,038 , GRCh38.p12 chr17: 47,255,278-47,255,672 ITGB3
    nsv4673962copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 45,379,443-45,382,341 , GRCh38 chr17: 47,302,077-47,304,975 ITGB3, EFCAB13-DT
    nsv4575992mobile element insertion1nstd166human GRCh37.p13 chr17: 45,380,615-45,380,615 , GRCh38.p12 chr17: 47,303,249-47,303,249 ITGB3, EFCAB13-DT
    nsv4505550mobile element insertion1nstd166human GRCh37.p13 chr17: 45,338,790-45,338,790 , GRCh38.p12 chr17: 47,261,424-47,261,424 ITGB3
    nsv4502154mobile element insertion1nstd166human GRCh37.p13 chr17: 45,372,779-45,372,779 , GRCh38.p12 chr17: 47,295,413-47,295,413 ITGB3
    nsv4499362mobile element insertion1nstd166human GRCh37.p13 chr17: 45,329,427-45,329,427 , GRCh38.p12 chr17: 47,252,061-47,252,061 ITGB3
    nsv4436018complex substitution1nstd102humanUncertain significance GRCh37 chr17: 45,008,570-45,994,044 , GRCh38.p12 chr17: 46,931,204-47,916,678 CDC27, ITGB3, 30 more genes
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