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 131

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921828copy number variation1nstd209human GRCh38 chr11: 75,180,175-75,180,474 , GRCh37.p13 chr11: 74,891,220-74,891,519 SLCO2B1
    nsv5919093copy number variation1nstd209human GRCh38 chr11: 75,179,768-75,180,048 , GRCh37.p13 chr11: 74,890,813-74,891,093 SLCO2B1
    nsv5710397mobile element insertion1nstd211human GRCh38 chr11: 75,168,943-75,168,943 , GRCh37.p13 chr11: 74,879,988-74,879,988 SLCO2B1
    nsv5499779copy number variation1nstd206human GRCh38 chr11: 75,195,770-75,202,153 , GRCh37.p13 chr11: 74,906,815-74,913,198 SLCO2B1
    nsv5406289mobile element insertion1nstd206human GRCh38 chr11: 75,168,943-75,168,994 , GRCh37.p13 chr11: 74,879,988-74,880,039 SLCO2B1
    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
    nsv5264193copy number variation1nstd204human GRCh38.p13 chr11: 75,160,992-75,163,091 , GRCh37.p13 chr11: 74,872,037-74,874,136 SLCO2B1
    nsv5121597mobile element insertion1nstd203human GRCh38 chr11: 75,186,506-75,186,532 , GRCh37.p13 chr11: 74,897,551-74,897,577 SLCO2B1
    nsv4989057copy number variation1nstd200human GRCh38 chr11: 75,093,302-75,241,792 , GRCh37.p13 chr11: 74,804,347-74,952,837 OR2AT1P, LOC100421207, 6 more genes
    nsv4987329copy number variation1nstd200human GRCh38 chr11: 75,173,947-75,174,046 , GRCh37.p13 chr11: 74,884,992-74,885,091 SLCO2B1
    nsv4842553copy number variation1nstd200human GRCh37 chr11: 74,804,347-74,952,837 , GRCh38.p12 chr11: 75,093,302-75,241,792 OR2AT4, OR2AT1P, 6 more genes
    nsv4205340copy number variation1nstd166human GRCh37.p13 chr11: 74,804,347-74,952,837 , GRCh38.p12 chr11: 75,093,302-75,241,792 SLCO2B1, OR2AT4, 6 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
    nsv3902667copy number variation1nstd102humanBenign GRCh37 chr11: 74,806,005-74,949,403 , GRCh38.p12 chr11: 75,094,960-75,238,358 SLCO2B1, OR2AT1P, 5 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
    nsv3156543copy number variation1nstd151human GRCh37 chr11: 74,904,260-74,915,630 , GRCh38.p12 chr11: 75,193,215-75,204,585 TPBGL-AS1, SLCO2B1
    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