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Items: 1 to 20 of 547

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980231insertion1nstd209human GRCh38 chr20: 36,396,348-36,396,348 , GRCh37.p13 chr20: 35,024,751-35,024,751 DLGAP4
    nsv5966357copy number variation1nstd209human GRCh38 chr20: 36,390,760-36,390,857 , GRCh37.p13 chr20: 35,019,163-35,019,260 DLGAP4
    nsv5963219copy number variation1nstd209human GRCh38 chr20: 36,318,974-36,324,256 , GRCh37.p13 chr20: 34,947,377-34,952,659 , GRCh37.p13 chr20|NW_003871095.1: 23,636-28,918 DLGAP4
    nsv5961294copy number variation1nstd209human GRCh38 chr20: 36,406,460-36,406,509 , GRCh37.p13 chr20: 35,034,863-35,034,912 DLGAP4
    nsv5961214copy number variation1nstd209human GRCh38 chr20: 36,464,765-36,464,841 , GRCh37.p13 chr20: 35,093,168-35,093,244 DLGAP4
    nsv5957810copy number variation1nstd209human GRCh38 chr20: 36,392,491-36,392,585 , GRCh37.p13 chr20: 35,020,894-35,020,988 DLGAP4
    nsv5956120copy number variation1nstd209human GRCh38 chr20: 36,415,226-36,427,438 , GRCh37.p13 chr20: 35,043,629-35,055,841 DLGAP4
    nsv5949550copy number variation1nstd209human GRCh38 chr20: 36,513,252-36,513,575 , GRCh37.p13 chr20: 35,141,655-35,141,978 DLGAP4-AS1, DLGAP4
    nsv5878855copy number variation1nstd209human GRCh38 chr20: 36,415,264-36,427,337 , GRCh37.p13 chr20: 35,043,667-35,055,740 DLGAP4
    nsv5867740copy number variation1nstd209human GRCh38 chr20: 36,318,961-36,324,010 , GRCh37.p13 chr20|NW_003871095.1: 23,623-28,672 , GRCh37.p13 chr20: 34,947,364-34,952,413 DLGAP4
    nsv5711487mobile element insertion1nstd211human GRCh38 chr20: 36,524,126-36,524,126 , GRCh37.p13 chr20: 35,152,529-35,152,529 DLGAP4, DLGAP4-AS1
    nsv5711436mobile element insertion2nstd211human GRCh38 chr20: 36,322,200-36,322,200 , GRCh37.p13 chr20|NW_003871095.1: 26,862-26,862 , GRCh37.p13 chr20: 34,950,603-34,950,603 DLGAP4
    nsv5702097mobile element insertion1nstd211human GRCh38 chr20: 36,416,658-36,416,658 , GRCh37.p13 chr20: 35,045,061-35,045,061 DLGAP4
    nsv5695921mobile element insertion1nstd211human GRCh38 chr20: 36,527,809-36,527,809 , GRCh37.p13 chr20: 35,156,212-35,156,212 DLGAP4, DLGAP4-AS1
    nsv5672455insertion1nstd207human GRCh38 chr20: 36,396,348-36,396,348 , GRCh37.p13 chr20: 35,024,751-35,024,751 DLGAP4
    nsv5671850insertion1nstd207human GRCh38 chr20: 36,314,370-36,314,370 , GRCh37.p13 chr20|NW_003871095.1: 19,032-19,032 DLGAP4
    nsv5671578insertion1nstd207human GRCh38 chr20: 36,360,686-36,360,686 , GRCh37.p13 chr20|NW_003871095.1: 65,348-65,348 , GRCh37.p13 chr20: 34,989,089-34,989,089 DLGAP4
    nsv5669496insertion1nstd207human GRCh38 chr20: 36,320,000-36,320,000 , GRCh37.p13 chr20|NW_003871095.1: 24,662-24,662 , GRCh37.p13 chr20: 34,948,403-34,948,403 DLGAP4
    nsv5594546copy number variation1nstd207human GRCh38 chr20: 36,392,491-36,392,585 , GRCh37.p13 chr20: 35,020,894-35,020,988 DLGAP4
    nsv5560305sequence alteration1nstd206human GRCh38 chr20: 36,507,286-36,660,208 , GRCh37.p13 chr20: 35,135,689-35,288,611 , MYL9, 8 more genes
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