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 490

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098902copy number variation1nstd102humanPathogenic GRCh37 chr16: 86,544,176-88,110,267 , GRCh38.p12 chr16: 86,510,570-88,076,661 LOC107984816, BANP, 33 more genes
    nsv7095106copy number variation1nstd102humanUncertain significance GRCh37 chr16: 87,960,334-87,960,571 , GRCh38.p12 chr16: 87,926,728-87,926,965 CA5A
    nsv7095105copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 87,935,498-87,938,530 , GRCh38.p12 chr16: 87,901,892-87,904,924 CA5A
    nsv7094699copy number variation2nstd102humanUncertain significance GRCh37 chr16: 87,636,753-90,109,753 , GRCh38.p12 chr16: 87,603,147-90,043,345 HSALR1, LOC105371412, 87 more genes
    nsv7094606copy number variation1nstd102humanUncertain significance GRCh37 chr16: 87,677,844-88,505,740 , GRCh38.p12 chr16: 87,644,238-88,439,332 MIR6775, LOC107984816, 15 more genes
    nsv7068827inversion1nstd229human GRCh38 chr16: 87,644,134-88,268,671 , GRCh37.p13 chr16: 87,677,740-88,302,277 BANP, LOC107984816, 13 more genes
    nsv6997653copy number variation1nstd229human GRCh38 chr16: 87,930,895-87,941,104 , GRCh37.p13 chr16: 87,964,501-87,974,710 CA5A
    nsv6995414copy number variation1nstd229human GRCh38 chr16: 87,933,486-87,937,910 , GRCh37.p13 chr16: 87,967,092-87,971,516 CA5A
    nsv6994765copy number variation1nstd229human GRCh38 chr16: 87,714,306-88,014,908 , GRCh37.p13 chr16: 87,747,912-88,048,514 LOC105371399, SLC7A5, 7 more genes
    nsv6993639copy number variation1nstd229human GRCh38 chr16: 87,865,949-87,903,359 , GRCh37.p13 chr16: 87,899,555-87,936,965 CA5A, SLC7A5
    nsv6993249copy number variation1nstd229human GRCh38 chr16: 87,920,998-87,938,006 , GRCh37.p13 chr16: 87,954,604-87,971,612 CA5A
    nsv6992173copy number variation1nstd229human GRCh38 chr16: 87,886,878-87,898,798 , GRCh37.p13 chr16: 87,920,484-87,932,404 CA5A
    nsv6991125copy number variation1nstd229human GRCh38 chr16: 87,909,563-87,909,600 , GRCh37.p13 chr16: 87,943,169-87,943,206 CA5A
    nsv6989357copy number variation1nstd229human GRCh38 chr16: 87,915,526-87,931,129 , GRCh37.p13 chr16: 87,949,132-87,964,735 CA5A
    nsv6984031copy number variation1nstd229human GRCh38 chr16: 87,895,801-87,901,300 , GRCh37.p13 chr16: 87,929,407-87,934,906 CA5A
    nsv6983112copy number variation1nstd229human GRCh38 chr16: 87,917,743-87,917,805 , GRCh37.p13 chr16: 87,951,349-87,951,411 CA5A
    nsv6981831copy number variation1nstd229human GRCh38 chr16: 87,930,960-87,931,441 , GRCh37.p13 chr16: 87,964,566-87,965,047 CA5A
    nsv6978833copy number variation1nstd229human GRCh38 chr16: 87,926,401-87,930,300 , GRCh37.p13 chr16: 87,960,007-87,963,906 CA5A
    nsv6637822copy number variation1nstd102humanUncertain significance GRCh37 chr16: 87,782,799-88,150,144 , GRCh38.p12 chr16: 87,749,193-88,116,538 KLHDC4, LOC105371399, 8 more genes
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 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