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 471

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073945inversion1nstd229human GRCh38 chr11: 90,173,116-90,244,860 , GRCh37.p13 chr11: 89,906,284-89,978,028 CHORDC1, NAALAD2
    nsv7072301inversion1nstd229human GRCh38 chr11: 89,705,504-90,174,109 , GRCh37.p13 chr11: 89,438,672-89,907,277 TRIM77, LOC642579, 24 more genes
    nsv7072045inversion1nstd229human GRCh38 chr11: 89,933,609-90,162,412 , GRCh37.p13 chr11: 89,666,777-89,895,580 TRIM64EP, LOC100128800, 9 more genes
    nsv7071690inversion1nstd229human GRCh38 chr11: 89,575,988-90,302,831 , GRCh37.p13 chr11: 89,309,156-90,035,999 TRIM64, UBTFL2, 30 more genes
    nsv7067654inversion1nstd229human GRCh38 chr11: 90,153,137-90,172,569 , GRCh37.p13 chr11: 89,886,305-89,905,737 NAALAD2
    nsv7065005inversion1nstd229human GRCh38 chr11: 90,170,065-90,191,887 , GRCh37.p13 chr11: 89,903,233-89,925,055 NAALAD2
    nsv7060154inversion1nstd229human GRCh38 chr11: 89,626,991-96,425,689 , GRCh37.p13 chr11: 89,360,159-96,158,853 LINC02756, OSBPL9P2, 119 more genes
    nsv6917854copy number variation1nstd229human GRCh38 chr11: 90,161,200-90,161,247 , GRCh37.p13 chr11: 89,894,368-89,894,415 NAALAD2
    nsv6917500copy number variation1nstd229human GRCh38 chr11: 90,139,338-90,291,765 , GRCh37.p13 chr11: 89,872,506-90,024,933 CHORDC1, TUBAP2, 2 more genes
    nsv6914931copy number variation1nstd229human GRCh38 chr11: 90,144,417-90,176,125 , GRCh37.p13 chr11: 89,877,585-89,909,293 NAALAD2
    nsv6914121copy number variation1nstd229human GRCh38 chr11: 89,708,489-94,988,932 , GRCh37.p13 chr11: 89,441,657-94,611,845 SNORA40, PIWIL4-AS1, 89 more genes
    nsv6909228copy number variation1nstd229human GRCh38 chr11: 90,104,081-90,182,201 , GRCh37.p13 chr11: 89,837,249-89,915,369 NAALAD2
    nsv6909221copy number variation1nstd229human GRCh38 chr11: 90,128,562-90,134,392 , GRCh37.p13 chr11: 89,861,730-89,867,560 NAALAD2
    nsv6908295copy number variation1nstd229human GRCh38 chr11: 90,144,423-90,144,516 , GRCh37.p13 chr11: 89,877,591-89,877,684 NAALAD2
    nsv6907879copy number variation1nstd229human GRCh38 chr11: 90,140,180-90,140,366 , GRCh37.p13 chr11: 89,873,348-89,873,534 NAALAD2
    nsv6907347copy number variation1nstd229human GRCh38 chr11: 89,715,432-96,566,090 , GRCh37.p13 chr11: 89,448,600-96,287,584 DISC1FP1, RPL32P25, 120 more genes
    nsv6906874copy number variation1nstd229human GRCh38 chr11: 90,183,081-90,183,293 , GRCh37.p13 chr11: 89,916,249-89,916,461 NAALAD2
    nsv6905717copy number variation1nstd229human GRCh38 chr11: 90,171,558-90,186,015 , GRCh37.p13 chr11: 89,904,726-89,919,183 NAALAD2
    nsv6905168copy number variation1nstd229human GRCh38 chr11: 90,187,801-90,190,300 , GRCh37.p13 chr11: 89,920,969-89,923,468 NAALAD2
    nsv6904570copy number variation1nstd229human GRCh38 chr11: 90,112,489-90,199,252 , GRCh37.p13 chr11: 89,845,657-89,932,420 CHORDC1, NAALAD2
    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