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 198

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094019copy number variation1nstd102humanUncertain significance GRCh37 chr11: 88,027,174-89,018,142 , GRCh38.p12 chr11: 88,294,006-89,284,974 GRM5, RNU6-16P, 5 more genes
    nsv7069436inversion1nstd229human GRCh38 chr11: 85,936,971-89,461,473 , GRCh37.p13 chr11: 85,648,014-89,194,641 , RNU6-1135P, 45 more genes
    nsv6917057copy number variation1nstd229human GRCh38 chr11: 88,334,501-88,366,800 , GRCh37.p13 chr11: 88,067,669-88,099,968 CTSC, LOC101929174
    nsv6913748copy number variation1nstd229human GRCh38 chr11: 88,182,152-88,370,144 , GRCh37.p13 chr11: 87,915,320-88,103,312 CTSC, LOC101929174
    nsv6911976copy number variation1nstd229human GRCh38 chr11: 88,321,448-88,324,221 , GRCh37.p13 chr11: 88,054,616-88,057,389 CTSC
    nsv6907681copy number variation1nstd229human GRCh38 chr11: 88,223,355-88,425,298 , GRCh37.p13 chr11: 87,956,523-88,158,466 CTSC, GAPDHP70, 1 more genes
    nsv6906463copy number variation1nstd229human GRCh38 chr11: 88,314,311-88,317,141 , GRCh37.p13 chr11: 88,047,479-88,050,309 CTSC
    nsv6904628copy number variation1nstd229human GRCh38 chr11: 88,148,852-88,322,170 , GRCh37.p13 chr11: 87,882,020-88,055,338 RAB38, CTSC, 1 more genes
    nsv6903906copy number variation1nstd229human GRCh38 chr11: 87,885,428-88,321,307 , GRCh37.p13 chr11: 87,596,320-88,054,475 LOC107984361, RAB38, 2 more genes
    nsv6900850copy number variation1nstd229human GRCh38 chr11: 87,282,559-88,311,721 , GRCh37.p13 chr11: 86,993,601-88,044,889 TMEM135, LOC107984361, 9 more genes
    nsv6899156copy number variation1nstd229human GRCh38 chr11: 88,323,101-88,376,300 , GRCh37.p13 chr11: 88,056,269-88,109,468 CTSC, LOC101929174
    nsv6637847copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,562,738-88,663,067 , GRCh38.p12 chr11: 80,851,695-88,929,899 PRSS23, MTCO3P25, 92 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6462157copy number variation1nstd223human GRCh38 chr11: 88,331,244-88,331,949 , GRCh37.p13 chr11: 88,064,412-88,065,117 CTSC
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6313961copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717 MTND5P38, XIAPP2, 252 more genes
    nsv6309387copy number variation1nstd102humanPathogenic GRCh37 chr11: 88,045,475-88,071,056 , GRCh38.p12 chr11: 88,312,307-88,337,888 CTSC, LOC101929174
    nsv6309386copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 88,040,961-88,042,398 , GRCh38.p12 chr11: 88,307,793-88,309,230 CTSC
    nsv6309385copy number variation1nstd102humanUncertain significance GRCh37 chr11: 88,027,174-88,029,452 , GRCh38.p12 chr11: 88,294,006-88,296,284 CTSC
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 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