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 160

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7028166copy number variation1nstd229human GRCh38 chr20: 35,637,750-35,647,955 , GRCh37.p13 chr20: 34,225,672-34,235,877 CPNE1, RNU6-759P, 2 more genes
    nsv7021198copy number variation1nstd229human GRCh38 chr20: 33,145,032-41,995,765 , GRCh37.p13 chr20: 31,732,838-40,624,405 PXMP4, RPL12P11, 199 more genes
    nsv7019999copy number variation1nstd229human GRCh38 chr20: 35,486,342-36,114,422 , GRCh37.p13 chr20: 34,074,168-34,702,344 HMGB3P2, NFS1, 24 more genes
    nsv6637725copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,833,535-34,815,537 , GRCh38.p12 chr20: 31,245,732-36,227,615 AHCY, ASIP, 160 more genes
    nsv6637546copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323 AHCY, ASIP, 195 more genes
    nsv6524164copy number variation1nstd223human GRCh38 chr20: 35,643,572-35,647,140 , GRCh37.p13 chr20: 34,231,494-34,235,062 RN7SKP271, CPNE1, 2 more genes
    nsv6311078copy number variation1nstd102humanPathogenic GRCh37 chr20: 31,189,994-34,287,210 , GRCh38.p12 chr20: 32,602,192-35,699,288 EDEM2, EIF2S2, 93 more genes
    nsv6133913copy number variation1nstd213human GRCh37 chr20: 33,870,000-34,270,001 , GRCh38.p12 chr20: 35,282,197-35,682,079 EIF6, GDF5, 18 more genes
    nsv6111579insertion1nstd212human GRCh38 chr20: 35,656,816-35,656,816 , GRCh37.p13 chr20: 34,244,738-34,244,738 RBM12, CPNE1
    nsv5978641insertion1nstd209human GRCh38 chr20: 35,656,817-35,656,817 , GRCh37.p13 chr20: 34,244,739-34,244,739 CPNE1, RBM12
    nsv5961542copy number variation1nstd209human GRCh38 chr20: 35,631,172-35,647,530 , GRCh37.p13 chr20: 34,219,094-34,235,452 CPNE1, RBM12, 2 more genes
    nsv5876061copy number variation1nstd209human GRCh38 chr20: 35,640,729-35,647,053 , GRCh37.p13 chr20: 34,228,651-34,234,975 RN7SKP271, RBM12, 2 more genes
    nsv5557509sequence alteration1nstd206human GRCh38 chr20: 35,627,992-36,077,048 , GRCh37.p13 chr20: 34,215,914-34,664,970 CPNE1, PHF20, 16 more genes
    nsv5538468insertion1nstd206human GRCh38 chr20: 35,656,829-35,656,867 , GRCh37.p13 chr20: 34,244,751-34,244,789 CPNE1, RBM12
    nsv5529788copy number variation1nstd206human GRCh38 chr20: 35,653,267-35,653,334 , GRCh37.p13 chr20: 34,241,189-34,241,256 CPNE1, RBM12
    nsv5028442copy number variation1nstd200human GRCh38 chr20: 35,637,749-35,647,955 , GRCh37.p13 chr20: 34,225,671-34,235,877 RNU6-759P, RBM12, 2 more genes
    nsv5022343copy number variation1nstd200human GRCh38 chr20: 32,602,560-45,347,064 , GRCh37.p13 chr20: 31,190,362-43,975,704 , SNHG11, 286 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv5022326copy number variation1nstd200human GRCh38 chr20: 32,216,214-44,981,731 , GRCh37.p13 chr20: 30,804,017-43,610,372 , HNF4A, 279 more genes
    nsv4868712copy number variation1nstd200human GRCh37 chr20: 34,225,671-34,235,877 , GRCh38.p12 chr20: 35,637,749-35,647,955 RNU6-759P, RN7SKP271, 2 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