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 87

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5499463copy number variation1nstd206human GRCh38 chr11: 10,441,892-10,512,161 , GRCh37.p13 chr11: 10,463,439-10,533,708 RNF141, MTRNR2L8, 2 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4672662copy number variation1nstd186human GRCh37 chr11: 10,529,488-10,534,969 , GRCh38.p12 chr11: 10,507,941-10,513,422 AMPD3, RNF141, 2 more genes
    nsv4665675copy number variation1nstd186human GRCh37 chr11: 10,529,348-10,531,585 , GRCh38.p12 chr11: 10,507,801-10,510,038 AMPD3, RNF141, 2 more genes
    nsv4609905copy number variation2nstd183human GRCh37 chr11: 10,529,348-10,531,585 , GRCh38.p12 chr11: 10,507,801-10,510,038 AMPD3, RNF141, 2 more genes
    nsv4607457copy number variation1nstd183human GRCh37 chr11: 10,529,055-10,531,585 , GRCh38.p12 chr11: 10,507,508-10,510,038 MIR4485, RNF141, 2 more genes
    nsv4602348copy number variation1nstd183human GRCh37 chr11: 10,529,470-10,531,983 , GRCh38.p12 chr11: 10,507,923-10,510,436 MTRNR2L8, AMPD3, 2 more genes
    nsv4599258copy number variation1nstd183human GRCh37 chr11: 10,529,488-10,534,969 , GRCh38.p12 chr11: 10,507,941-10,513,422 RNF141, MIR4485, 2 more genes
    nsv4415558copy number variation1nstd174human GRCh37 chr11: 10,529,039-10,532,011 , GRCh38.p12 chr11: 10,507,492-10,510,464 AMPD3, MTRNR2L8, 2 more genes
    nsv4367321copy number variation1nstd173human GRCh37 chr11: 9,422,923-11,175,143 , GRCh38.p12 chr11: 9,401,376-11,153,596 , LOC107984309, 40 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv4195609copy number variation1nstd166human GRCh37.p13 chr11: 10,511,057-10,539,114 , GRCh38.p12 chr11: 10,489,510-10,517,567 MIR4485, MTRNR2L8, 2 more genes
    nsv3919565copy number variation1nstd102humanPathogenic GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092 OR51A7, OR51F5P, 437 more genes
    nsv3915585copy number variation1nstd102humanPathogenic NCBI36 chr11: 9,967,639-16,803,929 , GRCh37 chr11: 10,011,063-16,847,353 , GRCh38 chr11: 9,989,516-16,825,806 BTBD10, LOC107984370, 86 more genes
    nsv3912558copy number variation1nstd102humanPathogenic GRCh37 chr11: 446,754-18,926,289 , GRCh38 chr11: 446,754-18,904,742 , NCBI36 chr11: 436,754-18,882,865 TRIM22, CSNK2A3, 546 more genes
    nsv3912175copy number variation1nstd102humanPathogenic NCBI36 chr11: 10,107,142-14,047,625 , GRCh37.p13 chr11: 10,150,566-14,091,049 , GRCh38.p12 chr11: 10,129,019-14,069,502 LINC02545, CENPUP1, 58 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3906221copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673 PCNAP4, LIN7C, 688 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