U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 73

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3897085copy number variation1nstd102humanBenign GRCh37 chr16: 8,942,216-8,956,703 , GRCh38.p12 chr16: 8,848,359-8,862,846 CARHSP1, LOC100130283, 1 more genes
    nsv4729219copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,958,907-9,232,888 , GRCh38.p12 chr16: 8,865,050-9,139,031 CARHSP1, USP7-AS1, 3 more genes
    nsv3896067copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,899,897-9,050,878 , GRCh38.p12 chr16: 8,806,040-8,957,021 CARHSP1, LOC100130283, 3 more genes
    nsv4350523copy number variation1nstd102humanPathogenic GRCh37 chr16: 8,839,796-9,728,670 , GRCh38.p12 chr16: 8,745,939-9,634,813 CARHSP1, LOC105371075, 15 more genes
    nsv7098957copy number variation1nstd102humanPathogenic GRCh37 chr16: 8,160,554-9,074,348 , GRCh38.p12 chr16: 8,110,552-8,980,491 CARHSP1, ABAT, 14 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 CARHSP1, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 CARHSP1, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 CARHSP1, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 CARHSP1, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 CARHSP1, FTLP14, 1868 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 CARHSP1, LOC105371069, 654 more genes
    nsv1398297copy number variation1nstd102humanPathogenic GRCh37 chr16: 102,839-28,327,676 , GRCh38.p12 chr16: 52,839-28,316,355 CARHSP1, BMERB1, 701 more genes
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 CARHSP1, NPIPB9, 597 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 CARHSP1, MIR6511B2, 535 more genes
    nsv3910441copy number variation1nstd102humanPathogenic NCBI36 chr16: 4,634,894-29,089,642 , GRCh37 chr16: 4,694,893-29,182,141 , GRCh38 chr16: 4,644,892-29,170,820 CARHSP1, LOC729945, 450 more genes
    nsv3903116copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-22,442,007 , GRCh38.p12 chr16: 35,880-22,430,686 CARHSP1, NPIPA8, 616 more genes
    nsv3900978copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-19,806,921 , GRCh38.p12 chr16: 35,880-19,795,599 CARHSP1, LOC105371091, 543 more genes
    nsv3915829copy number variation1nstd102humanPathogenic NCBI36 chr16: 656,663-15,744,462 , GRCh38 chr16: 666,662-15,743,104 , GRCh37 chr16: 716,662-15,836,961 CARHSP1, RPL35AP34, 429 more genes
    nsv3923267copy number variation1nstd102humanPathogenic GRCh37 chr16: 93,732-13,420,663 , GRCh38 chr16: 43,732-13,326,806 , NCBI36 chr16: 33,732-13,328,164 CARHSP1, METRN, 413 more genes
    nsv3917929copy number variation1nstd102humanPathogenic GRCh37 chr16: 96,766-11,619,372 , GRCh38 chr16: 46,766-11,525,516 , NCBI36 chr16: 36,766-11,526,873 CARHSP1, LOC100130283, 386 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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