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 291

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096700copy number variation1nstd102humanUncertain significance GRCh37 chr3: 15,643,358-15,687,154 , GRCh38.p12 chr3: 15,601,851-15,645,647 BTD, HACL1
    nsv7096544copy number variation1nstd102humanPathogenic GRCh37 chr3: 15,512,023-15,687,154 , GRCh38.p12 chr3: 15,470,516-15,645,647 BTD, RN7SL110P, 3 more genes
    nsv6714027copy number variation1nstd229human GRCh38 chr3: 15,573,301-15,583,400 , GRCh37.p13 chr3: 15,614,808-15,624,907 HACL1
    nsv6713100copy number variation1nstd229human GRCh38 chr3: 15,359,925-17,364,956 , GRCh37.p13 chr3: 15,401,432-17,406,448 RNU6-1024P, COLQ, 27 more genes
    nsv6712034copy number variation1nstd229human GRCh38 chr3: 14,670,901-15,564,100 , GRCh37.p13 chr3: 14,712,408-15,605,607 COLQ, RNU6-1024P, 22 more genes
    nsv6709348copy number variation1nstd229human GRCh38 chr3: 15,561,511-15,574,160 , GRCh37.p13 chr3: 15,603,018-15,615,667 HACL1
    nsv6707110copy number variation1nstd229human GRCh38 chr3: 15,593,102-15,597,177 , GRCh37.p13 chr3: 15,634,609-15,638,684 HACL1
    nsv6706135copy number variation1nstd229human GRCh38 chr3: 15,594,394-15,595,506 , GRCh37.p13 chr3: 15,635,901-15,637,013 HACL1
    nsv6705615copy number variation1nstd229human GRCh38 chr3: 15,572,285-15,591,484 , GRCh37.p13 chr3: 15,613,792-15,632,991 HACL1
    nsv6704607copy number variation1nstd229human GRCh38 chr3: 15,592,065-15,592,113 , GRCh37.p13 chr3: 15,633,572-15,633,620 HACL1
    nsv6636922copy number variation1nstd102humanUncertain significance GRCh37 chr3: 15,511,615-15,612,393 , GRCh38.p12 chr3: 15,470,108-15,570,886 MIR4270, HACL1, 2 more genes
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 TMEM43, SLC6A6, 132 more genes
    nsv6545239inversion1nstd223human GRCh38 chr3: 15,588,174-15,588,399 , GRCh37.p13 chr3: 15,629,681-15,629,906 HACL1
    nsv6544033inversion1nstd223human GRCh38 chr3: 15,593,757-15,594,321 , GRCh37.p13 chr3: 15,635,264-15,635,828 HACL1
    nsv6543579inversion1nstd223human GRCh38 chr3: 15,583,687-15,584,526 , GRCh37.p13 chr3: 15,625,194-15,626,033 HACL1
    nsv6542023inversion1nstd223human GRCh38 chr3: 15,558,821-15,559,206 , GRCh37.p13 chr3: 15,600,328-15,600,713 HACL1
    nsv6541766inversion1nstd223human GRCh38 chr3: 15,575,605-15,576,015 , GRCh37.p13 chr3: 15,617,112-15,617,522 HACL1
    nsv6370384copy number variation1nstd223human GRCh38 chr3: 15,573,836-15,575,683 , GRCh37.p13 chr3: 15,615,343-15,617,190 HACL1
    nsv6365525copy number variation1nstd223human GRCh38 chr3: 15,593,901-15,595,800 , GRCh37.p13 chr3: 15,635,408-15,637,307 HACL1
    nsv6315249copy number variation1nstd102humanPathogenic GRCh38 chr3: 13,371,737-20,095,506 , GRCh37.p13 chr3: 13,413,237-20,136,998 RNU6-905P, PRR3P1, 99 more genes
    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