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 306

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959986insertion1nstd209human GRCh38 chr1: 225,808,718-225,808,718 , GRCh37.p13 chr1: 225,996,420-225,996,420 EPHX1
    nsv5884342copy number variation1nstd209human GRCh38 chr1: 221,964,560-227,275,238 , GRCh37.p13 chr1: 222,137,902-227,462,939 , YBX1P9, 111 more genes
    nsv5882984copy number variation1nstd209human GRCh38 chr1: 225,815,112-225,815,438 , GRCh37.p13 chr1: 226,002,814-226,003,140 EPHX1
    nsv5879093copy number variation1nstd209human GRCh38 chr1: 225,819,063-225,819,241 , GRCh37.p13 chr1: 226,006,765-226,006,943 EPHX1
    nsv5877044copy number variation1nstd209human GRCh38 chr1: 225,830,996-225,831,058 , GRCh37.p13 chr1: 226,018,697-226,018,759 EPHX1
    nsv5873176copy number variation1nstd209human GRCh38 chr1: 225,830,620-225,830,709 , GRCh37.p13 chr1: 226,018,321-226,018,410 EPHX1
    nsv5688197mobile element insertion2nstd211human GRCh38 chr1: 225,808,731-225,808,731 , GRCh37.p13 chr1: 225,996,433-225,996,433 EPHX1
    nsv5687216mobile element insertion1nstd211human GRCh38 chr1: 225,834,589-225,834,589 , GRCh37.p13 chr1: 226,022,290-226,022,290 EPHX1
    nsv5617014insertion1nstd207human GRCh38 chr1: 225,808,718-225,808,718 , GRCh37.p13 chr1: 225,996,420-225,996,420 EPHX1
    nsv5607812insertion1nstd207human GRCh38 chr1: 225,821,570-225,821,570 , GRCh37.p13 chr1: 226,009,271-226,009,271 EPHX1
    nsv5580132copy number variation1nstd207human GRCh38 chr1: 225,815,112-225,815,438 , GRCh37.p13 chr1: 226,002,814-226,003,140 EPHX1
    nsv5576639copy number variation1nstd207human GRCh38 chr1: 225,819,063-225,819,241 , GRCh37.p13 chr1: 226,006,765-226,006,943 EPHX1
    nsv5445653copy number variation1nstd206human GRCh38 chr1: 225,830,625-225,830,710 , GRCh37.p13 chr1: 226,018,326-226,018,411 EPHX1
    nsv5442792copy number variation1nstd206human GRCh38 chr1: 225,815,115-225,815,439 , GRCh37.p13 chr1: 226,002,817-226,003,141 EPHX1
    nsv5438331copy number variation1nstd206human GRCh38 chr1: 225,841,516-225,841,836 , GRCh37.p13 chr1: 226,029,217-226,029,537 TMEM63A, EPHX1
    nsv5434427copy number variation1nstd206human GRCh38 chr1: 225,819,076-225,819,242 , GRCh37.p13 chr1: 226,006,778-226,006,944 EPHX1
    nsv5411950mobile element insertion1nstd206human GRCh38 chr1: 225,808,718-225,808,718 , GRCh37.p13 chr1: 225,996,420-225,996,420 EPHX1
    nsv5382510copy number variation2nstd186human GRCh37 chr1: 226,002,817-226,003,141 , GRCh38.p12 chr1: 225,815,115-225,815,439 EPHX1
    nsv5381973copy number variation1nstd186human GRCh37 chr1: 226,006,779-226,006,943 , GRCh38.p12 chr1: 225,819,077-225,819,241 EPHX1
    nsv5381912copy number variation1nstd186human GRCh37 chr1: 226,006,778-226,006,944 , GRCh38.p12 chr1: 225,819,076-225,819,242 EPHX1
    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