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 284

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7097416copy number variation1nstd102humanPathogenic GRCh37 chr8: 117,859,739-120,844,804 , GRCh38.p12 chr8: 116,847,500-119,832,564 SAMD12, LOC105375717, 38 more genes
    nsv7097415copy number variation1nstd102humanUncertain significance GRCh37 chr8: 117,647,788-120,797,526 , GRCh38.p12 chr8: 116,635,549-119,785,286 LOC100286746, LOC105375717, 40 more genes
    nsv7072142inversion1nstd229human GRCh38 chr8: 113,332,988-120,659,210 , GRCh37.p13 chr8: 114,345,217-121,671,450 ENPP2, RAD21-AS1, 67 more genes
    nsv6842956copy number variation1nstd229human GRCh38 chr8: 116,534,905-116,857,852 , GRCh37.p13 chr8: 117,547,143-117,870,091 UTP23, LOC112268030, 4 more genes
    nsv6838335copy number variation1nstd229human GRCh38 chr8: 116,494,722-116,896,714 , GRCh37.p13 chr8: 117,506,960-117,908,953 MIR3610, LOC105375713, 6 more genes
    nsv6637773copy number variation1nstd102humanUncertain significance GRCh37 chr8: 117,617,532-117,862,147 , GRCh38.p12 chr8: 116,605,293-116,849,908 RAD21, LOC105375713, 4 more genes
    nsv6637224copy number variation1nstd102humanPathogenic GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133 RNU4-37P, LOC100420215, 220 more genes
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634633copy number variation1nstd102humanPathogenic GRCh37 chr8: 117,860,986-117,861,652 , GRCh38 chr8: 116,848,747-116,849,413 RAD21
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6434255copy number variation1nstd223human GRCh38 chr8: 116,854,201-116,856,200 , GRCh37.p13 chr8: 117,866,440-117,868,439 RAD21
    nsv6426176copy number variation1nstd223human GRCh38 chr8: 116,872,001-116,876,600 , GRCh37.p13 chr8: 117,884,240-117,888,839 RAD21, RAD21-AS1, 1 more genes
    nsv6424271copy number variation1nstd223human GRCh38 chr8: 116,606,390-116,854,663 , GRCh37.p13 chr8: 117,618,629-117,866,902 RAD21, LOC112268030, 4 more genes
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6312897copy number variation1nstd102humanUncertain significance GRCh37 chr8: 117,574,515-117,878,968 , GRCh38.p12 chr8: 116,562,277-116,866,729 LOC112268030, LOC105375712, 4 more genes
    nsv6312389copy number variation1nstd102humanUncertain significance GRCh37 chr8: 117,859,739-117,866,727 , GRCh38.p12 chr8: 116,847,500-116,854,488 RAD21
    nsv6303823copy number variation1nstd186human GRCh37 chr8: 117,882,461-117,882,520 , GRCh38.p12 chr8: 116,870,222-116,870,281 RAD21
    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