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 93

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5913364copy number variation1nstd209human GRCh38 chr11: 68,689,990-68,690,238 , GRCh37.p13 chr11: 68,457,458-68,457,706 GAL
    nsv5554536sequence alteration1nstd206human GRCh38 chr11: 68,686,213-68,687,167 , GRCh37.p13 chr11: 68,453,681-68,454,635 GAL, LOC107984343
    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
    nsv5373692translocation1nstd200human GRCh38 chr11: 68,686,232-68,686,232 , GRCh38 chr11: 68,687,057-68,687,057 , GRCh37.p13 chr11: 68,453,700-68,453,700 , GRCh37.p13 chr11: 68,454,525-68,454,525 LOC107984343, GAL
    nsv5331683translocation1nstd200human GRCh37 chr11: 68,453,700-68,453,700 , GRCh37 chr11: 68,454,525-68,454,525 , GRCh38.p12 chr11: 68,686,232-68,686,232 , GRCh38.p12 chr11: 68,687,057-68,687,057 GAL, LOC107984343
    nsv5323205translocation1nstd204human GRCh37.p13 chr11: 68,453,700-68,453,700 , GRCh37.p13 chr11: 68,454,525-68,454,525 , GRCh38.p13 chr11: 68,686,232-68,686,232 , GRCh38.p13 chr11: 68,687,057-68,687,057 GAL, LOC107984343
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4715326copy number variation1nstd195human GRCh37 chr11: 68,355,451-69,089,801 , GRCh38.p12 chr11: 68,587,983-69,322,333 , CPT1A, 19 more genes
    nsv4705829copy number variation1nstd195human GRCh37 chr11: 68,244,001-68,627,601 , GRCh38.p12 chr11: 68,476,533-68,860,133 CPT1A, TESMIN, 4 more genes
    nsv4682061copy number variation1nstd102humanUncertain significance GRCh37 chr11: 68,452,372-68,458,475 , GRCh38.p12 chr11: 68,684,904-68,691,007 GAL, LOC107984343
    nsv4675823copy number variation1nstd102humanUncertain significance GRCh37 chr11: 68,266,294-68,515,741 , GRCh38.p12 chr11: 68,498,826-68,748,273 PPP6R3, GAL, 2 more genes
    nsv4528628copy number variation1nstd166human GRCh37.p13 chr11: 68,306,151-68,837,546 , GRCh38.p12 chr11: 68,538,683-69,070,078 GAL, LOC107984343, 10 more genes
    nsv4528066copy number variation1nstd166human GRCh37.p13 chr11: 68,147,730-68,454,934 , GRCh38.p12 chr11: 68,380,262-68,687,466 GAL, LOC107984343, 3 more genes
    nsv4380475copy number variation1nstd173human GRCh37 chr11: 68,330,757-68,458,521 , GRCh38.p12 chr11: 68,563,289-68,691,053 LOC107984343, PPP6R3, 1 more genes
    nsv4365299copy number variation1nstd173human GRCh37 chr11: 68,326,633-68,458,521 , GRCh38.p12 chr11: 68,559,165-68,691,053 LOC107984343, GAL, 1 more genes
    nsv4199876copy number variation1nstd166human GRCh37.p13 chr11: 68,392,382-68,480,426 , GRCh38.p12 chr11: 68,624,914-68,712,958 GAL, LOC107984343, 1 more genes
    nsv3956511insertion1nstd168human GRCh38 chr11: 68,643,456-68,683,411 , GRCh37.p13 chr11: 68,410,924-68,450,879 LOC107984343, GAL
    nsv3955190copy number variation1nstd168human GRCh38 chr11: 68,599,413-68,683,411 , GRCh37.p13 chr11: 68,366,881-68,450,879 GAL, LOC107984343, 1 more genes
    nsv3920906copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 66,741,311-68,972,547 , GRCh37 chr11: 66,984,735-69,263,366 , GRCh38 chr11: 67,217,264-69,448,598 GRK2, ALDH3B1, 82 more genes
    nsv3917463copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 67,555,736-70,982,189 , GRCh37 chr11: 67,799,160-71,304,541 , GRCh38 chr11: 68,031,693-71,593,495 CCND1, CHKA, 71 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    Support Center