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 440

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094800copy number variation1nstd102humanUncertain significance GRCh37 chr16: 11,647,369-11,647,565 , GRCh38.p12 chr16: 11,553,513-11,553,709 LITAF
    nsv7094607copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,829,597-11,683,693 , GRCh38.p12 chr16: 8,735,740-11,589,837 LOC400499, NUBP1, 58 more genes
    nsv7077549inversion1nstd229human GRCh38 chr16: 11,619,905-11,632,146 , GRCh37.p13 chr16: 11,713,761-11,726,002 LITAF
    nsv7076079inversion1nstd229human GRCh38 chr16: 9,015,595-14,846,246 , GRCh37.p13 chr16: 9,109,452-14,940,103 LOC105371093, RNU6-633P, 100 more genes
    nsv7069727inversion1nstd229human GRCh38 chr16: 11,611,301-11,623,677 , GRCh37.p13 chr16: 11,705,157-11,717,533 LITAF
    nsv7067421inversion1nstd229human GRCh38 chr16: 11,568,744-11,577,518 , GRCh37.p13 chr16: 11,662,600-11,671,374 LITAF
    nsv7063994inversion1nstd229human GRCh38 chr16: 11,592,177-11,624,816 , GRCh37.p13 chr16: 11,686,033-11,718,672 LITAF
    nsv7062963inversion1nstd229human GRCh38 chr16: 11,608,775-11,615,206 , GRCh37.p13 chr16: 11,702,631-11,709,062 LITAF
    nsv7062920inversion1nstd229human GRCh38 chr16: 11,546,319-11,550,163 , GRCh37.p13 chr16: 11,640,175-11,644,019 LITAF
    nsv7062684inversion1nstd229human GRCh38 chr16: 11,574,121-11,582,868 , GRCh37.p13 chr16: 11,667,977-11,676,724 LITAF
    nsv6974667copy number variation1nstd229human GRCh38 chr16: 11,569,943-11,578,543 , GRCh37.p13 chr16: 11,663,799-11,672,399 LITAF
    nsv6973929copy number variation1nstd229human GRCh38 chr16: 11,612,580-11,615,199 , GRCh37.p13 chr16: 11,706,436-11,709,055 LITAF
    nsv6973520copy number variation1nstd229human GRCh38 chr16: 11,629,069-11,629,123 , GRCh37.p13 chr16: 11,722,925-11,722,979 LITAF
    nsv6972753copy number variation1nstd229human GRCh38 chr16: 11,616,748-11,854,058 , GRCh37.p13 chr16: 11,710,604-11,947,915 LITAF, ZC3H7A, 5 more genes
    nsv6972275copy number variation1nstd229human GRCh38 chr16: 11,565,997-11,576,608 , GRCh37.p13 chr16: 11,659,853-11,670,464 LITAF
    nsv6971730copy number variation1nstd229human GRCh38 chr16: 11,445,040-11,738,730 , GRCh37.p13 chr16: 11,538,896-11,832,586 LOC101927131, LITAF, 3 more genes
    nsv6971322copy number variation1nstd229human GRCh38 chr16: 11,574,080-11,574,841 , GRCh37.p13 chr16: 11,667,936-11,668,697 LITAF
    nsv6971321copy number variation1nstd229human GRCh38 chr16: 11,634,651-11,642,497 , GRCh37.p13 chr16: 11,728,507-11,736,353 LITAF
    nsv6970722copy number variation1nstd229human GRCh38 chr16: 11,614,084-11,619,132 , GRCh37.p13 chr16: 11,707,940-11,712,988 LITAF
    nsv6969651copy number variation1nstd229human GRCh38 chr16: 11,619,962-11,630,238 , GRCh37.p13 chr16: 11,713,818-11,724,094 LITAF
    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