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 250

    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
    nsv7093777copy number variation1nstd102humanPathogenic GRCh37 chr10: 102,283,594-102,510,668 , GRCh38.p12 chr10: 100,523,837-100,750,911 NDUFB8, PAX2, 1 more genes
    nsv7065201inversion1nstd229human GRCh38 chr10: 100,756,732-100,762,239 , GRCh37.p13 chr10: 102,516,489-102,521,996 PAX2
    nsv7064309inversion1nstd229human GRCh38 chr10: 100,500,702-100,949,925 , GRCh37.p13 chr10: 102,260,459-102,709,682 HIF1AN, NDUFB8, 3 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
    nsv6893632copy number variation1nstd229human GRCh38 chr10: 100,764,272-100,777,934 , GRCh37.p13 chr10: 102,524,029-102,537,691 PAX2
    nsv6892564copy number variation1nstd229human GRCh38 chr10: 100,751,377-100,765,027 , GRCh37.p13 chr10: 102,511,134-102,524,784 PAX2
    nsv6889522copy number variation1nstd229human GRCh38 chr10: 100,810,542-100,816,381 , GRCh37.p13 chr10: 102,570,299-102,576,138 PAX2
    nsv6881573copy number variation1nstd229human GRCh38 chr10: 100,797,522-100,801,238 , GRCh37.p13 chr10: 102,557,279-102,560,995 PAX2
    nsv6879814copy number variation1nstd229human GRCh38 chr10: 100,774,245-100,777,248 , GRCh37.p13 chr10: 102,534,002-102,537,005 PAX2
    nsv6879661copy number variation1nstd229human GRCh38 chr10: 100,829,558-100,836,725 , GRCh37.p13 chr10: 102,589,315-102,596,482 PAX2
    nsv6636187copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 102,505,467-102,539,254 , GRCh38.p12 chr10: 100,745,710-100,779,497 PAX2
    nsv6620150copy number variation1nstd224human GRCh37 chr10: 102,533,297-102,705,243 , GRCh38.p12 chr10: 100,773,540-100,945,486 SLF2, PAX2
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6444859copy number variation1nstd223human GRCh38 chr10: 100,777,747-100,778,657 , GRCh37.p13 chr10: 102,537,504-102,538,414 PAX2
    nsv6440909copy number variation1nstd223human GRCh38 chr10: 100,810,542-100,816,377 , GRCh37.p13 chr10: 102,570,299-102,576,134 PAX2
    nsv6309051copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 102,539,235-102,569,013 , GRCh38.p12 chr10: 100,779,478-100,809,256 PAX2
    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