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 84

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4987277copy number variation1nstd200human GRCh38 chr11: 73,391,240-73,392,276 , GRCh37.p13 chr11: 73,102,285-73,103,321 RELT
    nsv4987276copy number variation1nstd200human GRCh38 chr11: 73,370,904-73,377,118 , GRCh37.p13 chr11: 73,081,949-73,088,163 RELT
    nsv4847044copy number variation1nstd200human GRCh37 chr11: 73,102,285-73,103,321 , GRCh38.p12 chr11: 73,391,240-73,392,276 RELT
    nsv4833526copy number variation1nstd200human GRCh37 chr11: 73,081,949-73,088,163 , GRCh38.p12 chr11: 73,370,904-73,377,118 RELT
    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
    nsv4208087copy number variation1nstd166human GRCh37.p13 chr11: 73,108,836-73,109,562 , GRCh38.p12 chr11: 73,397,791-73,398,517 RELT, FAM168A
    nsv4193013copy number variation1nstd166human GRCh37.p13 chr11: 73,093,500-73,100,000 , GRCh38.p12 chr11: 73,382,455-73,388,955 RELT
    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
    nsv3144311copy number variation1nstd151human GRCh37 chr11: 73,074,789-73,120,711 , GRCh38.p12 chr11: 73,363,744-73,409,666 RELT, FAM168A, 1 more genes
    nsv3142081copy number variation1nstd151human GRCh37 chr11: 71,668,270-74,638,536 , GRCh38.p12 chr11: 71,957,224-74,927,491 , RPL36AP38, 92 more genes
    nsv1596111short tandem repeat3nstd128human GRCh37 chr11: 73,088,727-73,088,746 , GRCh38.p12 chr11: 73,377,682-73,377,701 RELT
    nsv1596110short tandem repeat14nstd128human GRCh37 chr11: 73,088,315-73,088,338 , GRCh38.p12 chr11: 73,377,270-73,377,293 RELT
    nsv1594028short tandem repeat6nstd128human GRCh37 chr11: 73,097,993-73,098,008 , GRCh38.p12 chr11: 73,386,948-73,386,963 RELT
    nsv1593419short tandem repeat1nstd128human GRCh37 chr11: 73,089,724-73,089,735 , GRCh38.p12 chr11: 73,378,679-73,378,690 RELT
    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