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 168

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094672copy number variation1nstd102humanUncertain significance GRCh37 chr16: 46,694,384-48,258,199 , GRCh38.p12 chr16: 46,660,472-48,224,288 LOC100420642, ITFG1-AS1, 26 more genes
    nsv6995805copy number variation1nstd229human GRCh38 chr16: 48,142,185-48,144,916 , GRCh37.p13 chr16: 48,176,096-48,178,827 ABCC12
    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
    nsv6991229copy number variation1nstd229human GRCh38 chr16: 48,103,001-48,106,100 , GRCh37.p13 chr16: 48,136,912-48,140,011 ABCC12
    nsv6990464copy number variation1nstd229human GRCh38 chr16: 48,092,821-48,106,475 , GRCh37.p13 chr16: 48,126,732-48,140,386 ABCC12
    nsv6984761copy number variation1nstd229human GRCh38 chr16: 48,134,664-48,135,798 , GRCh37.p13 chr16: 48,168,575-48,169,709 ABCC12
    nsv6982354copy number variation1nstd229human GRCh38 chr16: 48,081,190-48,081,344 , GRCh37.p13 chr16: 48,115,101-48,115,255 ABCC12
    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
    nsv6505481copy number variation1nstd223human GRCh38 chr16: 47,983,720-48,159,925 , GRCh37.p13 chr16: 48,017,631-48,193,836 ABCC12
    nsv6502408copy number variation1nstd223human GRCh38 chr16: 48,092,841-48,106,505 , GRCh37.p13 chr16: 48,126,752-48,140,416 ABCC12
    nsv6500046copy number variation1nstd223human GRCh38 chr16: 48,092,547-48,093,662 , GRCh37.p13 chr16: 48,126,458-48,127,573 ABCC12
    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
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6132991copy number variation1nstd213human GRCh37 chr16: 46,460,000-48,129,895 , GRCh38.p12 chr16: 46,426,088-48,095,984 CKBP1, PHKB, 31 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5942508copy number variation1nstd209human GRCh38 chr16: 48,103,321-48,104,782 , GRCh37.p13 chr16: 48,137,232-48,138,693 ABCC12
    nsv5936784copy number variation1nstd209human GRCh38 chr16: 48,102,549-48,113,366 , GRCh37.p13 chr16: 48,136,460-48,147,277 ABCC12
    nsv5934878copy number variation1nstd209human GRCh38 chr16: 48,129,935-48,130,496 , GRCh37.p13 chr16: 48,163,846-48,164,407 ABCC12
    nsv5867572copy number variation1nstd209human GRCh38 chr16: 48,104,790-48,108,989 , GRCh37.p13 chr16: 48,138,701-48,142,900 ABCC12
    nsv5697450mobile element insertion2nstd211human GRCh38 chr16: 48,090,052-48,090,052 , GRCh37.p13 chr16: 48,123,963-48,123,963 ABCC12
    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