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 135

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5913360copy number variation1nstd209human GRCh38 chr11: 73,289,408-73,291,760 , GRCh37.p13 chr11: 73,000,453-73,002,805 P2RY6
    nsv5866843copy number variation1nstd209human GRCh38 chr11: 73,289,380-73,291,522 , GRCh37.p13 chr11: 73,000,425-73,002,567 P2RY6
    nsv5506591copy number variation1nstd206human GRCh38 chr11: 73,289,388-73,291,787 , GRCh37.p13 chr11: 73,000,433-73,002,832 P2RY6
    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
    nsv5339419translocation1nstd200human GRCh37 chr11: 73,010,007-73,010,007 , GRCh37 chr11: 73,009,860-73,009,860 , GRCh38.p12 chr11: 73,298,815-73,298,815 , GRCh38.p12 chr11: 73,298,962-73,298,962 P2RY6
    nsv5301435copy number variation1nstd204human GRCh38.p13 chr11: 73,298,789-73,298,987 , GRCh37.p13 chr11: 73,009,834-73,010,032 P2RY6
    nsv5271506copy number variation1nstd204human GRCh38.p13 chr11: 73,251,201-73,280,600 , GRCh37.p13 chr11: 72,962,246-72,991,645 P2RY6, LOC105369382
    nsv5128799mobile element insertion1nstd203human GRCh38 chr11: 73,274,496-73,274,540 , GRCh37.p13 chr11: 72,985,541-72,985,585 P2RY6
    nsv4987274copy number variation1nstd200human GRCh38 chr11: 73,278,189-73,279,256 , GRCh37.p13 chr11: 72,989,234-72,990,301 P2RY6
    nsv4837323copy number variation1nstd200human GRCh37 chr11: 72,989,234-72,990,301 , GRCh38.p12 chr11: 73,278,189-73,279,256 P2RY6
    nsv4707042copy number variation1nstd195human GRCh37 chr11: 72,963,001-73,006,951 , GRCh38.p12 chr11: 73,251,956-73,295,906 P2RY6, LOC105369382
    nsv4455208copy number variation1nstd102humanUncertain significance GRCh37 chr11: 72,998,686-73,156,844 , GRCh38.p12 chr11: 73,287,641-73,445,799 RELT, FAM168A, 3 more genes
    nsv4207341copy number variation1nstd166human GRCh37.p13 chr11: 72,962,336-72,981,145 , GRCh38.p12 chr11: 73,251,291-73,270,100 P2RY6, LOC105369382
    nsv4198853copy number variation1nstd166human GRCh37.p13 chr11: 73,000,453-73,002,812 , GRCh38.p12 chr11: 73,289,408-73,291,767 P2RY6
    nsv4195400copy number variation1nstd166human GRCh37.p13 chr11: 72,962,000-73,045,800 , GRCh38.p12 chr11: 73,250,955-73,334,755 ARHGEF17-AS1, P2RY6, 2 more genes
    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
    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