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 194

    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
    nsv7070015inversion1nstd229human GRCh38 chr10: 101,109,173-101,114,511 , GRCh37.p13 chr10: 102,868,930-102,874,268 TLX1NB
    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
    nsv7059134inversion1nstd229human GRCh38 chr10: 101,097,336-101,097,384 , GRCh37.p13 chr10: 102,857,093-102,857,141 TLX1NB
    nsv6896298copy number variation1nstd229human GRCh38 chr10: 100,883,101-101,090,000 , GRCh37.p13 chr10: 102,642,858-102,849,757 MIR608, LOC107984262, 9 more genes
    nsv6892494copy number variation1nstd229human GRCh38 chr10: 101,097,600-101,097,683 , GRCh37.p13 chr10: 102,857,357-102,857,440 TLX1NB
    nsv6891906copy number variation1nstd229human GRCh38 chr10: 101,134,195-101,134,504 , GRCh37.p13 chr10: 102,893,952-102,894,261 TLX1, TLX1NB
    nsv6890789copy number variation1nstd229human GRCh38 chr10: 101,101,181-101,101,279 , GRCh37.p13 chr10: 102,860,938-102,861,036 TLX1NB
    nsv6885761copy number variation1nstd229human GRCh38 chr10: 101,074,292-101,088,362 , GRCh37.p13 chr10: 102,834,049-102,848,119 TLX1NB
    nsv6885171copy number variation1nstd229human GRCh38 chr10: 101,023,532-101,227,683 , GRCh37.p13 chr10: 102,783,289-102,987,440 LOC107984262, LINC01514, 9 more genes
    nsv6884847copy number variation1nstd229human GRCh38 chr10: 101,086,357-101,167,450 , GRCh37.p13 chr10: 102,846,114-102,927,207 TLX1, RNY5P7, 1 more genes
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6579072inversion1nstd223human GRCh38 chr10: 101,107,659-101,111,032 , GRCh37.p13 chr10: 102,867,416-102,870,789 TLX1NB
    nsv6452078copy number variation1nstd223human GRCh38 chr10: 101,110,223-101,113,873 , GRCh37.p13 chr10: 102,869,980-102,873,630 TLX1NB
    nsv6450689copy number variation1nstd223human GRCh38 chr10: 101,136,430-101,167,629 , GRCh37.p13 chr10: 102,896,187-102,927,386 TLX1NB, RNY5P7, 1 more genes
    nsv6443422copy number variation1nstd223human GRCh38 chr10: 101,074,292-101,088,358 , GRCh37.p13 chr10: 102,834,049-102,848,115 TLX1NB
    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