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 220

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922345copy number variation1nstd209human GRCh38 chr11: 17,552,531-17,552,584 , GRCh37.p13 chr11: 17,574,078-17,574,131 OTOG
    nsv5917971copy number variation1nstd209human GRCh38 chr11: 17,582,745-17,583,040 , GRCh37.p13 chr11: 17,604,292-17,604,587 OTOG
    nsv5702864mobile element insertion1nstd211human GRCh38 chr11: 17,621,424-17,621,424 , GRCh37.p13 chr11: 17,642,971-17,642,971 OTOG
    nsv5696961mobile element insertion2nstd211human GRCh38 chr11: 17,577,719-17,577,719 , GRCh37.p13 chr11: 17,599,266-17,599,266 OTOG
    nsv5694975mobile element insertion1nstd211human GRCh38 chr11: 17,550,415-17,550,415 , GRCh37.p13 chr11: 17,571,962-17,571,962 OTOG
    nsv5661275insertion1nstd207human GRCh38 chr11: 17,639,896-17,639,896 , GRCh37.p13 chr11: 17,661,443-17,661,443 OTOG
    nsv5658907insertion1nstd207human GRCh38 chr11: 17,552,528-17,552,528 , GRCh37.p13 chr11: 17,574,075-17,574,075 OTOG
    nsv5658328insertion1nstd207human GRCh38 chr11: 17,577,704-17,577,704 , GRCh37.p13 chr11: 17,599,251-17,599,251 OTOG
    nsv5656439insertion1nstd207human GRCh38 chr11: 17,552,531-17,552,531 , GRCh37.p13 chr11: 17,574,078-17,574,078 OTOG
    nsv5647226insertion2nstd207human GRCh38 chr11: 17,552,549-17,552,549 , GRCh37.p13 chr11: 17,574,096-17,574,096 OTOG
    nsv5592650copy number variation1nstd207human GRCh38 chr11: 17,639,840-17,639,919 , GRCh37.p13 chr11: 17,661,387-17,661,466 OTOG
    nsv5549587insertion1nstd206human GRCh38 chr11: 17,639,938-17,639,947 , GRCh37.p13 chr11: 17,661,485-17,661,494 OTOG
    nsv5511473copy number variation1nstd206human GRCh38 chr11: 17,552,479-17,552,635 , GRCh37.p13 chr11: 17,574,026-17,574,182 OTOG
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    nsv5507463copy number variation1nstd206human GRCh38 chr11: 17,638,335-17,638,415 , GRCh37.p13 chr11: 17,659,882-17,659,962 OTOG
    nsv5411446mobile element insertion1nstd206human GRCh38 chr11: 17,577,719-17,577,770 , GRCh37.p13 chr11: 17,599,266-17,599,317 OTOG
    nsv5406204mobile element insertion1nstd206human GRCh38 chr11: 17,621,424-17,621,475 , GRCh37.p13 chr11: 17,642,971-17,643,022 OTOG
    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
    nsv5380720copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,552,691-19,213,995 , GRCh38.p12 chr11: 17,531,144-19,192,448 USH1C, HIGD1AP5, 53 more genes
    nsv5127106mobile element insertion1nstd203human GRCh38 chr11: 17,577,704-17,577,719 , GRCh37.p13 chr11: 17,599,251-17,599,266 OTOG
    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