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 223

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6997626copy number variation1nstd229human GRCh38 chr16: 48,588,201-48,592,300 , GRCh37.p13 chr16: 48,622,112-48,626,211 N4BP1
    nsv6996943copy number variation1nstd229human GRCh38 chr16: 48,571,503-48,574,920 , GRCh37.p13 chr16: 48,605,414-48,608,831 N4BP1
    nsv6992791copy number variation1nstd229human GRCh38 chr16: 48,586,613-48,597,688 , GRCh37.p13 chr16: 48,620,524-48,631,599 N4BP1
    nsv6992256copy number variation1nstd229human GRCh38 chr16: 47,725,786-49,432,895 , GRCh37.p13 chr16: 47,759,697-49,466,806 C16orf78, RNU6-257P, 24 more genes
    nsv6990552copy number variation1nstd229human GRCh38 chr16: 48,356,804-48,700,221 , GRCh37.p13 chr16: 48,390,715-48,734,132 MOCS1P1, SIAH1, 6 more genes
    nsv6990347copy number variation1nstd229human GRCh38 chr16: 48,543,263-48,546,146 , GRCh37.p13 chr16: 48,577,174-48,580,057 N4BP1
    nsv6990214copy number variation1nstd229human GRCh38 chr16: 48,606,359-48,608,777 , GRCh37.p13 chr16: 48,640,270-48,642,688 N4BP1
    nsv6988236copy number variation1nstd229human GRCh38 chr16: 48,604,561-48,604,646 , GRCh37.p13 chr16: 48,638,472-48,638,557 N4BP1
    nsv6986282copy number variation1nstd229human GRCh38 chr16: 48,593,864-48,597,043 , GRCh37.p13 chr16: 48,627,775-48,630,954 N4BP1
    nsv6637799copy number variation1nstd102humanUncertain significance GRCh37 chr16: 48,440,455-48,916,593 , GRCh38.p12 chr16: 48,406,544-48,882,682 RNU6-257P, MOCS1P1, 7 more genes
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6623629copy number variation1nstd224human GRCh37 chr16: 48,520,586-48,921,691 , GRCh38.p12 chr16: 48,486,675-48,887,780 N4BP1, MOCS1P1, 5 more genes
    nsv6514607copy number variation1nstd223human GRCh38 chr16: 48,589,398-48,590,009 , GRCh37.p13 chr16: 48,623,309-48,623,920 N4BP1
    nsv6501388copy number variation1nstd223human GRCh38 chr16: 48,571,501-48,574,919 , GRCh37.p13 chr16: 48,605,412-48,608,830 N4BP1
    nsv6501226copy number variation1nstd223human GRCh38 chr16: 48,588,246-48,592,483 , GRCh37.p13 chr16: 48,622,157-48,626,394 N4BP1
    nsv6496160copy number variation1nstd223human GRCh38 chr16: 48,589,501-48,592,300 , GRCh37.p13 chr16: 48,623,412-48,626,211 N4BP1
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6271204copy number variation1nstd214human GRCh38 chr16: 48,604,548-48,604,645 , GRCh37.p13 chr16: 48,638,459-48,638,556 N4BP1
    nsv6250256mobile element insertion1nstd215human GRCh38 chr16: 48,608,736-48,608,736 , GRCh37.p13 chr16: 48,642,647-48,642,647 N4BP1
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 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