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 118

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5590655copy number variation1nstd207human GRCh38 chr11: 75,409,956-75,410,033 , GRCh37.p13 chr11: 75,121,000-75,121,077 RPS3
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5366979translocation1nstd200human GRCh38 chr11: 75,408,343-75,408,343 , GRCh38 chr3: 9,587,085-9,587,085 , GRCh37.p13 chr11: 75,119,387-75,119,387 , GRCh37.p13 chr3: 9,628,769-9,628,769 RPS3
    nsv4987341copy number variation1nstd200human GRCh38 chr11: 75,411,660-75,413,461 , GRCh37.p13 chr11: 75,122,704-75,124,505 RPS3
    nsv4987340copy number variation1nstd200human GRCh38 chr11: 75,405,830-75,408,581 , GRCh37.p13 chr11: 75,116,874-75,119,625 RPS3
    nsv4837402copy number variation1nstd200human GRCh37 chr11: 75,122,704-75,124,505 , GRCh38.p12 chr11: 75,411,660-75,413,461 RPS3
    nsv4740152copy number variation1nstd199human GRCh37 chr11: 75,120,863-75,120,991 , GRCh38.p12 chr11: 75,409,819-75,409,947 RPS3
    nsv4527220copy number variation1nstd166human GRCh37.p13 chr11: 75,107,594-75,108,545 , GRCh38.p12 chr11: 75,396,550-75,397,501 RPS3
    nsv4389902copy number variation1nstd171human GRCh37 chr11: 75,120,443-75,120,479 , GRCh38.p12 chr11: 75,409,399-75,409,435 RPS3
    nsv4211382copy number variation1nstd166human GRCh37.p13 chr11: 75,121,044-75,121,531 , GRCh38.p12 chr11: 75,410,000-75,410,487 RPS3
    nsv4204490copy number variation1nstd166human GRCh37.p13 chr11: 75,121,023-75,121,078 , GRCh38.p12 chr11: 75,409,979-75,410,034 RPS3
    nsv4194282copy number variation1nstd166human GRCh37.p13 chr11: 75,111,962-75,112,293 , GRCh38.p12 chr11: 75,400,918-75,401,249 SNORD15A, RPS3
    nsv3916301copy number variation1nstd102humanPathogenic GRCh38 chr11: 71,928,796-77,064,521 , GRCh37 chr11: 71,639,842-76,751,808 , NCBI36 chr11: 71,317,490-76,453,216 RN7SL786P, LIPT2-AS1, 146 more genes
    nsv3915804copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895 TPBGL, MAP6, 173 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
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3898361copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202 SESN3, LOC107984352, 694 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3334117mobile element deletion2nstd162human GRCh38 chr11: 75,409,958-75,410,035 , GRCh37.p13 chr11: 75,121,002-75,121,079 RPS3
    nsv3152618copy number variation1nstd151human GRCh37 chr11: 74,985,115-75,115,915 , GRCh38.p12 chr11: 75,274,071-75,404,871 SNORD15B, MIR326, 3 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