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 636

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094178copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,983,971-65,984,266 , GRCh38.p12 chr11: 66,216,500-66,216,795 PACS1
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv7093935copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,006,255-66,010,751 , GRCh38.p12 chr11: 66,238,784-66,243,280 PACS1
    nsv7075070inversion1nstd229human GRCh38 chr11: 66,119,113-66,137,952 , GRCh37.p13 chr11: 65,886,584-65,905,423 PACS1
    nsv7071124inversion1nstd229human GRCh38 chr11: 66,156,077-66,164,413 , GRCh37.p13 chr11: 65,923,548-65,931,884 PACS1
    nsv7063793inversion1nstd229human GRCh38 chr11: 66,156,620-66,161,652 , GRCh37.p13 chr11: 65,924,091-65,929,123 PACS1
    nsv7061449inversion1nstd229human GRCh38 chr11: 65,331,281-66,115,058 , GRCh37.p13 chr11: 65,098,752-65,882,529 LOC100420020, LINC02736, 53 more genes
    nsv7058327inversion1nstd229human GRCh38 chr11: 66,073,537-66,073,592 , GRCh37.p13 chr11: 65,841,008-65,841,063 PACS1
    nsv6917584copy number variation1nstd229human GRCh38 chr11: 66,156,971-66,166,928 , GRCh37.p13 chr11: 65,924,442-65,934,399 PACS1
    nsv6917447copy number variation1nstd229human GRCh38 chr11: 66,195,897-66,195,943 , GRCh37.p13 chr11: 65,963,368-65,963,414 PACS1
    nsv6917099copy number variation1nstd229human GRCh38 chr11: 66,099,972-66,107,486 , GRCh37.p13 chr11: 65,867,443-65,874,957 PACS1
    nsv6916304copy number variation1nstd229human GRCh38 chr11: 66,091,515-66,092,369 , GRCh37.p13 chr11: 65,858,986-65,859,840 PACS1
    nsv6916170copy number variation1nstd229human GRCh38 chr11: 66,171,719-66,180,799 , GRCh37.p13 chr11: 65,939,190-65,948,270 PACS1
    nsv6916058copy number variation1nstd229human GRCh38 chr11: 66,178,151-66,178,249 , GRCh37.p13 chr11: 65,945,622-65,945,720 PACS1
    nsv6915292copy number variation1nstd229human GRCh38 chr11: 66,244,407-66,252,722 , GRCh37.p13 chr11: 66,011,878-66,020,193 PACS1
    nsv6914921copy number variation1nstd229human GRCh38 chr11: 65,667,113-66,107,104 , GRCh37.p13 chr11: 65,434,584-65,874,575 SNX32, OVOL1, 28 more genes
    nsv6914617copy number variation1nstd229human GRCh38 chr11: 66,166,419-66,171,864 , GRCh37.p13 chr11: 65,933,890-65,939,335 PACS1
    nsv6913079copy number variation1nstd229human GRCh38 chr11: 66,137,704-66,140,909 , GRCh37.p13 chr11: 65,905,175-65,908,380 PACS1
    nsv6910723copy number variation1nstd229human GRCh38 chr11: 66,181,325-66,190,659 , GRCh37.p13 chr11: 65,948,796-65,958,130 PACS1, LOC105369354
    nsv6909807copy number variation1nstd229human GRCh38 chr11: 66,205,801-66,208,400 , GRCh37.p13 chr11: 65,973,272-65,975,871 PACS1
    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