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 88

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094183copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083 LOC112268078, LRTOMT, 142 more genes
    nsv6908275copy number variation1nstd229human GRCh38 chr11: 71,281,500-72,194,614 , GRCh37.p13 chr11: 71,088,949-71,905,658 DEFB130C, ANAPC15, 40 more genes
    nsv6637545copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,777,538-72,144,933 , GRCh38.p12 chr11: 72,066,492-72,433,889 CLPB, FOLR3, 15 more genes
    nsv6470560copy number variation1nstd223human GRCh38 chr11: 72,025,209-72,302,197 , GRCh37.p13 chr11: 71,736,255-72,013,241 CLPB, FOLR3, 14 more genes
    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
    nsv6314007copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,567,724-72,488,649 , GRCh38.p12 chr11: 71,856,678-72,777,604 STARD10, PDE2A, 38 more genes
    nsv6289694insertion1nstd214human GRCh38 chr11: 72,100,065-72,100,065 , GRCh37.p13 chr11: 71,811,111-71,811,111 LRTOMT, LAMTOR1
    nsv6248184mobile element insertion1nstd215human GRCh38 chr11: 72,101,854-72,101,854 , GRCh37.p13 chr11: 71,812,900-71,812,900 LAMTOR1, LRTOMT
    nsv5927114copy number variation1nstd209human GRCh38 chr11: 72,098,858-72,099,109 , GRCh37.p13 chr11: 71,809,904-71,810,155 LRTOMT, LAMTOR1
    nsv5912882copy number variation1nstd209human GRCh38 chr11: 72,099,255-72,103,180 , GRCh37.p13 chr11: 71,810,301-71,814,226 LAMTOR1, LRTOMT
    nsv5911308copy number variation1nstd209human GRCh38 chr11: 72,098,415-72,098,779 , GRCh37.p13 chr11: 71,809,461-71,809,825 LRTOMT, LAMTOR1
    nsv5908624copy number variation1nstd209human GRCh38 chr11: 72,097,912-72,098,285 , GRCh37.p13 chr11: 71,808,958-71,809,331 LAMTOR1, LRTOMT
    nsv5511944copy number variation1nstd206human GRCh38 chr11: 72,098,418-72,098,733 , GRCh37.p13 chr11: 71,809,464-71,809,779 LAMTOR1, LRTOMT
    nsv5501878copy number variation1nstd206human GRCh38 chr11: 72,097,917-72,098,286 , GRCh37.p13 chr11: 71,808,963-71,809,332 LRTOMT, LAMTOR1
    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
    nsv5343053translocation1nstd200human GRCh37 chr11: 71,809,332-71,809,332 , GRCh37 chr11: 71,808,963-71,808,963 , GRCh38.p12 chr11: 72,097,917-72,097,917 , GRCh38.p12 chr11: 72,098,286-72,098,286 LAMTOR1, LRTOMT
    nsv5338189translocation1nstd200human GRCh37 chr11: 71,810,304-71,810,304 , GRCh37 chr11: 97,741,756-97,741,756 , GRCh38.p12 chr11: 72,099,258-72,099,258 , GRCh38.p12 chr11: 97,870,756-97,870,756 LRTOMT, LAMTOR1
    nsv5325943translocation1nstd204human GRCh37.p13 chr11: 71,809,464-71,809,464 , GRCh37.p13 chr11: 71,809,826-71,809,826 , GRCh38.p13 chr11: 72,098,418-72,098,418 , GRCh38.p13 chr11: 72,098,780-72,098,780 LAMTOR1, LRTOMT
    nsv5322279translocation1nstd204human GRCh37.p13 chr11: 71,808,963-71,808,963 , GRCh37.p13 chr11: 71,809,332-71,809,332 , GRCh38.p13 chr11: 72,097,917-72,097,917 , GRCh38.p13 chr11: 72,098,286-72,098,286 LAMTOR1, LRTOMT
    nsv5278677copy number variation1nstd204human GRCh37.p13 chr11: 71,772,747-71,889,344 , GRCh38.p13 chr11: 72,061,701-72,178,300 FOLR3, NUMA1, 7 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