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 330

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138570copy number variation1nstd232human GRCh37.p13 chr15: 40,896,391-40,896,442 , GRCh38.p12 chr15: 40,604,193-40,604,244 KNL1
    nsv7077186inversion1nstd229human GRCh38 chr15: 35,051,912-40,816,689 , GRCh37.p13 chr15: 35,344,113-41,108,887 BUB1B-PAK6, LOC751603, 96 more genes
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv7059694inversion1nstd229human GRCh38 chr15: 40,604,635-40,642,730 , GRCh37.p13 chr15: 40,896,833-40,934,928 RN7SL376P, KNL1
    nsv7059363inversion1nstd229human GRCh38 chr15: 40,487,055-41,342,774 , GRCh37.p13 chr15: 40,779,254-41,634,972 DLL4, CHP1, 33 more genes
    nsv6969691copy number variation1nstd229human GRCh38 chr15: 40,593,953-40,595,009 , GRCh37.p13 chr15: 40,886,151-40,887,207 TRS-GCT4-2, KNL1
    nsv6966287copy number variation1nstd229human GRCh38 chr15: 40,627,672-40,634,874 , GRCh37.p13 chr15: 40,919,870-40,927,072 KNL1
    nsv6964883copy number variation1nstd229human GRCh38 chr15: 39,883,301-41,010,600 , GRCh37.p13 chr15: 40,175,502-41,302,798 SRP14, BUB1B-PAK6, 54 more genes
    nsv6964666copy number variation1nstd229human GRCh38 chr15: 40,530,252-40,731,066 , GRCh37.p13 chr15: 40,822,451-41,023,264 CCDC32, MRPL42P5, 6 more genes
    nsv6595384inversion1nstd223human GRCh38 chr15: 40,658,863-40,659,502 , GRCh37.p13 chr15: 40,951,061-40,951,700 KNL1
    nsv6594331inversion1nstd223human GRCh38 chr15: 40,662,860-40,663,050 , GRCh37.p13 chr15: 40,955,058-40,955,248 KNL1
    nsv6593454inversion1nstd223human GRCh38 chr15: 40,629,701-40,631,053 , GRCh37.p13 chr15: 40,921,899-40,923,251 KNL1
    nsv6590908inversion1nstd223human GRCh38 chr15: 40,596,399-40,596,932 , GRCh37.p13 chr15: 40,888,597-40,889,130 KNL1
    nsv6589736inversion1nstd223human GRCh38 chr15: 40,633,070-40,633,818 , GRCh37.p13 chr15: 40,925,268-40,926,016 KNL1
    nsv6589296inversion1nstd223human GRCh38 chr15: 40,637,953-40,638,756 , GRCh37.p13 chr15: 40,930,151-40,930,954 KNL1
    nsv6587929inversion1nstd223human GRCh38 chr15: 40,633,188-40,633,707 , GRCh37.p13 chr15: 40,925,386-40,925,905 KNL1
    nsv6587428inversion1nstd223human GRCh38 chr15: 40,596,800-40,597,584 , GRCh37.p13 chr15: 40,888,998-40,889,782 KNL1
    nsv6586767inversion1nstd223human GRCh38 chr15: 40,615,653-40,616,063 , GRCh37.p13 chr15: 40,907,851-40,908,261 KNL1, RN7SL376P
    nsv6582626inversion1nstd223human GRCh38 chr15: 40,639,021-40,639,500 , GRCh37.p13 chr15: 40,931,219-40,931,698 KNL1
    nsv6578003inversion1nstd223human GRCh38 chr15: 40,637,781-40,638,749 , GRCh37.p13 chr15: 40,929,979-40,930,947 KNL1
    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