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 98

    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
    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
    nsv6893021copy number variation1nstd229human GRCh38 chr10: 100,528,429-100,531,764 , GRCh37.p13 chr10: 102,288,186-102,291,521 NDUFB8
    nsv6888806copy number variation1nstd229human GRCh38 chr10: 100,519,811-100,527,396 , GRCh37.p13 chr10: 102,279,568-102,287,153 SEC31B, NDUFB8
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6453002copy number variation1nstd223human GRCh38 chr10: 100,512,435-100,608,282 , GRCh37.p13 chr10: 102,272,192-102,368,039 HIF1AN, SEC31B, 1 more genes
    nsv6450994copy number variation1nstd223human GRCh38 chr10: 100,528,429-100,531,760 , GRCh37.p13 chr10: 102,288,186-102,291,517 NDUFB8
    nsv6132013copy number variation1nstd213human GRCh37 chr10: 101,250,000-103,200,001 , GRCh38.p12 chr10: 99,490,243-101,440,244 CHUK, ABCC2, 52 more genes
    nsv6131925copy number variation2nstd213human GRCh37 chr10: 101,250,000-103,190,001 , GRCh38.p12 chr10: 99,490,243-101,430,244 CHUK, ABCC2, 52 more genes
    nsv6131845copy number variation1nstd213human GRCh37 chr10: 100,150,000-103,440,001 , GRCh38.p12 chr10: 98,390,243-101,680,244 CHUK, ABCC2, 70 more genes
    nsv5492004copy number variation1nstd206human GRCh38 chr10: 100,517,442-100,523,134 , GRCh37.p13 chr10: 102,277,199-102,282,891 NDUFB8, SEC31B
    nsv5491286copy number variation1nstd206human GRCh38 chr10: 100,528,429-100,531,760 , GRCh37.p13 chr10: 102,288,186-102,291,517 NDUFB8
    nsv4970295copy number variation1nstd200human GRCh38 chr10: 100,528,424-100,531,760 , GRCh37.p13 chr10: 102,288,181-102,291,517 NDUFB8
    nsv4674975copy number variation1nstd102humanUncertain significance GRCh37 chr10: 101,932,457-102,392,841 , GRCh38.p12 chr10: 100,172,700-100,633,084 NDUFB8, SNORA12, 12 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