U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 352

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978760insertion1nstd209human GRCh38 chr17: 20,360,249-20,360,249 , GRCh37.p13 chr17: 20,263,562-20,263,562 CCDC144CP
    nsv5933579copy number variation1nstd209human GRCh38 chr17: 16,936,959-20,558,118 , GRCh37.p13 chr17: 16,840,273-20,461,431 , FAM106B, 146 more genes
    nsv5886828copy number variation1nstd209human GRCh38 chr17: 20,360,351-20,403,348 , GRCh37.p13 chr17: 20,263,664-20,306,661 UPF3AP2, CCDC144CP
    nsv5881084copy number variation1nstd209human GRCh38 chr17: 20,347,830-20,349,329 , GRCh37.p13 chr17: 20,251,143-20,252,642 CCDC144CP
    nsv5880095copy number variation1nstd209human GRCh38 chr17: 20,286,311-20,341,491 , GRCh37.p13 chr17: 20,189,624-20,244,804 RNU6-1057P, RNU6-467P, 2 more genes
    nsv5877730copy number variation1nstd209human GRCh38 chr17: 20,384,767-20,391,404 , GRCh37.p13 chr17: 20,288,080-20,294,717 CCDC144CP
    nsv5874982copy number variation1nstd209human GRCh38 chr17: 20,391,405-20,411,634 , GRCh37.p13 chr17: 20,294,718-20,314,947 CCDC144CP, USP32P3
    nsv5874300copy number variation2nstd209human GRCh38 chr17: 20,349,627-20,359,718 , GRCh37.p13 chr17: 20,252,940-20,263,031 CCDC144CP
    nsv5868711copy number variation2nstd209human GRCh38 chr17: 20,356,665-20,358,718 , GRCh37.p13 chr17: 20,259,978-20,262,031 CCDC144CP
    nsv5710956mobile element insertion1nstd211human GRCh38 chr17: 20,397,758-20,397,758 , GRCh37.p13 chr17: 20,301,071-20,301,071 CCDC144CP
    nsv5710955mobile element insertion1nstd211human GRCh38 chr17: 20,351,152-20,351,152 , GRCh37.p13 chr17: 20,254,465-20,254,465 CCDC144CP
    nsv5705773mobile element insertion1nstd211human GRCh38 chr17: 20,397,932-20,397,932 , GRCh37.p13 chr17: 20,301,245-20,301,245 CCDC144CP
    nsv5705170mobile element insertion1nstd211human GRCh38 chr17: 20,369,248-20,369,248 , GRCh37.p13 chr17: 20,272,561-20,272,561 CCDC144CP
    nsv5702356mobile element insertion2nstd211human GRCh38 chr17: 20,391,940-20,391,940 , GRCh37.p13 chr17: 20,295,253-20,295,253 CCDC144CP
    nsv5700975mobile element insertion1nstd211human GRCh38 chr17: 20,338,967-20,338,967 , GRCh37.p13 chr17: 20,242,280-20,242,280 CCDC144CP
    nsv5697603mobile element insertion1nstd211human GRCh38 chr17: 20,351,139-20,351,139 , GRCh37.p13 chr17: 20,254,452-20,254,452 CCDC144CP
    nsv5670902inversion1nstd207human GRCh37.p13 chr17: 19,143,942-21,250,947 , GRCh38 chr17: 19,240,629-21,558,840 , ALDH3A1, 86 more genes
    nsv5664122insertion1nstd207human GRCh38 chr17: 20,322,534-20,322,534 , GRCh37.p13 chr17: 20,225,847-20,225,847 RNU6-467P, CCDC144CP
    nsv5662435insertion1nstd207human GRCh38 chr17: 20,372,700-20,372,700 , GRCh37.p13 chr17: 20,276,013-20,276,013 CCDC144CP
    nsv5660188insertion1nstd207human GRCh38 chr17: 20,356,761-20,356,761 , GRCh37.p13 chr17: 20,260,074-20,260,074 CCDC144CP
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center