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 101

    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
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7093699copy number variation1nstd102humanUncertain significance GRCh37 chr10: 102,747,968-103,535,657 , GRCh38.p12 chr10: 100,988,211-101,775,900 RNY5P7, TLX1, 25 more genes
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6897727copy number variation1nstd229human GRCh38 chr10: 101,666,701-101,878,800 , GRCh37.p13 chr10: 103,426,458-103,638,557 , LOC105378457, 10 more genes
    nsv6897419copy number variation1nstd229human GRCh38 chr10: 101,770,591-101,938,935 , GRCh37.p13 chr10: 103,530,348-103,698,692 LOC101927445, ARMH3, 6 more genes
    nsv6896348copy number variation1nstd229human GRCh38 chr10: 101,779,466-101,782,656 , GRCh37.p13 chr10: 103,539,223-103,542,413 FGF8, NPM3, 1 more genes
    nsv6886137copy number variation1nstd229human GRCh38 chr10: 101,764,816-101,789,165 , GRCh37.p13 chr10: 103,524,573-103,548,922 OGA, LOC105378457, 3 more genes
    nsv6881128copy number variation1nstd229human GRCh38 chr10: 101,769,718-101,769,781 , GRCh37.p13 chr10: 103,529,475-103,529,538 LOC105378457, FGF8
    nsv6878827copy number variation1nstd229human GRCh38 chr10: 101,779,763-101,779,855 , GRCh37.p13 chr10: 103,539,520-103,539,612 NPM3, FGF8
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6309052copy number variation1nstd102humanUncertain significance GRCh37 chr10: 102,987,027-103,530,396 , GRCh38.p12 chr10: 101,227,270-101,770,639 FBXW4, RNU2-59P, 14 more genes
    nsv5131986mobile element insertion1nstd203human GRCh38 chr10: 101,771,271-101,771,281 , GRCh37.p13 chr10: 103,531,028-103,531,038 LOC105378457, FGF8
    nsv4970343copy number variation1nstd200human GRCh38 chr10: 101,769,718-101,769,781 , GRCh37.p13 chr10: 103,529,475-103,529,538 FGF8, LOC105378457
    nsv4680797copy number variation1nstd189human GRCh37.p13 chr10: 102,835,750-103,653,301 , GRCh38.p12 chr10: 101,075,993-101,893,544 , FGF8, 28 more genes
    nsv4484285mobile element insertion1nstd166human GRCh37.p13 chr10: 103,531,028-103,531,028 , GRCh38.p12 chr10: 101,771,271-101,771,271 LOC105378457, FGF8
    nsv4349819copy number variation1nstd102humanPathogenic GRCh37 chr10: 102,822,575-103,558,868 , GRCh38.p12 chr10: 101,062,818-101,799,111 LBX1, TLX1, 22 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 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