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 96

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7077571inversion1nstd229human GRCh38 chr10: 104,332,100-105,414,338 , GRCh37.p13 chr10: 106,091,858-107,174,096 SORCS3, SORCS3-AS1, 7 more genes
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv6891851copy number variation1nstd229human GRCh38 chr10: 103,994,859-104,941,952 , GRCh37.p13 chr10: 105,754,617-106,701,710 LOC105378464, GSTO1, 16 more genes
    nsv6882174copy number variation1nstd229human GRCh38 chr10: 104,338,222-105,010,713 , GRCh37.p13 chr10: 106,097,980-106,770,471 SORCS3-AS1, CFAP58, 5 more genes
    nsv6880434copy number variation1nstd229human GRCh38 chr10: 103,302,516-106,977,869 , GRCh37.p13 chr10: 105,062,273-108,737,627 RNU11-3P, GSTO2, 48 more genes
    nsv6879126copy number variation1nstd229human GRCh38 chr10: 104,461,080-104,928,323 , GRCh37.p13 chr10: 106,220,838-106,688,081 SORCS3-AS1, LOC105378464, 2 more genes
    nsv6590725inversion1nstd223human GRCh38 chr10: 104,471,183-104,474,027 , GRCh37.p13 chr10: 106,230,941-106,233,785 LINC02620
    nsv6589983inversion1nstd223human GRCh38 chr10: 104,332,098-105,414,336 , GRCh37.p13 chr10: 106,091,856-107,174,094 SORCS3, ITPRIP, 7 more genes
    nsv6313984copy number variation1nstd102humanUncertain significance GRCh37 chr10: 106,147,023-106,318,823 , GRCh38.p12 chr10: 104,387,265-104,559,065 LINC02620, CFAP58
    nsv6003418copy number variation1nstd212human GRCh38 chr10: 104,479,795-104,479,857 , GRCh37.p13 chr10: 106,239,553-106,239,615 LINC02620
    nsv5313105copy number variation1nstd204human GRCh37.p13 chr10: 106,152,481-106,294,781 , GRCh38.p13 chr10: 104,392,723-104,535,023 CFAP58, LINC02620
    nsv5252304copy number variation1nstd204human GRCh38.p13 chr10: 104,462,347-104,494,180 , GRCh37.p13 chr10: 106,222,105-106,253,938 LINC02620
    nsv4834234copy number variation1nstd200human GRCh37 chr10: 106,152,509-106,294,754 , GRCh38.p12 chr10: 104,392,751-104,534,996 LINC02620, CFAP58
    nsv4738776copy number variation1nstd199human GRCh37 chr10: 106,239,532-106,239,642 , GRCh38.p12 chr10: 104,479,774-104,479,884 LINC02620
    nsv4528498copy number variation1nstd166human GRCh37.p13 chr10: 106,048,999-106,289,000 , GRCh38.p12 chr10: 104,289,241-104,529,242 ITPRIP, GSTO2, 4 more genes
    nsv4344837sequence alteration1nstd166human GRCh37.p13 chr10: 106,230,940-106,233,784 , GRCh38.p12 chr10: 104,471,182-104,474,026 LINC02620
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 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