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 832

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112816copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,887,031-16,308,753 , GRCh38.p12 chr16: 14,793,174-16,214,896 , GRCh38.p12 chr16|NT_187607.1: 326,909-1,872,893 NTAN1, MIR3179-1, 50 more genes
    nsv6112786copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,124,782-16,291,779 , GRCh38.p12 chr16: 15,030,925-16,197,922 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,855,918 RNU6-213P, LOC105371102, 25 more genes
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5929838copy number variation1nstd209human GRCh38 chr16: 15,882,355-15,930,402 , GRCh37.p13 chr16: 15,976,212-16,024,259 CEP20, RPL15P20, 1 more genes
    nsv5928138copy number variation1nstd209human GRCh38 chr16: 15,180,124-18,091,718 , GRCh37.p13 chr16: 15,273,981-18,185,575 , LOC102723692, 42 more genes
    nsv5887412copy number variation1nstd209human GRCh38 chr16: 15,862,621-15,864,220 , GRCh37.p13 chr16: 15,956,478-15,958,077 CEP20
    nsv5877019copy number variation1nstd209human GRCh38 chr16: 15,887,014-15,901,362 , GRCh37.p13 chr16: 15,980,871-15,995,219 CEP20, LOC107984869
    nsv5875655copy number variation2nstd209human GRCh38 chr16: 15,887,015-15,888,113 , GRCh37.p13 chr16: 15,980,872-15,981,970 CEP20
    nsv5717612mobile element insertion1nstd211human GRCh38 chr16: 15,876,810-15,876,810 , GRCh37.p13 chr16: 15,970,667-15,970,667 CEP20, RNU6-213P
    nsv5701900mobile element insertion1nstd211human GRCh38 chr16: 15,872,800-15,872,800 , GRCh37.p13 chr16: 15,966,657-15,966,657 CEP20
    nsv5700550mobile element insertion2nstd211human GRCh38 chr16: 15,869,879-15,869,879 , GRCh37.p13 chr16: 15,963,736-15,963,736 CEP20
    nsv5647049insertion1nstd207human GRCh38 chr16: 15,869,864-15,869,864 , GRCh37.p13 chr16: 15,963,721-15,963,721 CEP20
    nsv5523724copy number variation1nstd206human GRCh38 chr16: 15,885,536-15,885,637 , GRCh37.p13 chr16: 15,979,393-15,979,494 CEP20
    nsv5424151mobile element insertion1nstd206human GRCh38 chr16: 15,869,879-15,869,930 , GRCh37.p13 chr16: 15,963,736-15,963,787 CEP20
    nsv5423217mobile element insertion1nstd206human GRCh38 chr16: 15,872,800-15,872,851 , GRCh37.p13 chr16: 15,966,657-15,966,708 CEP20
    nsv5392017copy number variation1nstd186human GRCh37 chr16: 15,976,173-16,024,297 , GRCh38.p12 chr16: 15,882,316-15,930,440 , GRCh38.p12 chr16|NT_187607.1: 1,540,311-1,588,404 CEP20, RPL15P20, 1 more genes
    nsv5391030copy number variation1nstd186human GRCh37 chr16: 15,976,172-16,024,297 , GRCh38.p12 chr16: 15,882,315-15,930,440 , GRCh38.p12 chr16|NT_187607.1: 1,540,310-1,588,404 CEP20, RPL15P20, 1 more genes
    nsv5381790copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,126,890-16,293,190 , GRCh38.p12 chr16: 15,033,033-16,199,333 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,857,331 RRN3, CEP20, 25 more genes
    nsv5380994copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,758,636-16,292,059 , GRCh38.p12 chr16|NT_187607.1: 1,322,790-1,856,198 , GRCh38.p12 chr16: 15,664,779-16,198,202 RPL15P20, ABCC1, 7 more genes
    nsv5380983copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,968,859-16,363,239 , GRCh38.p12 chr16: 14,875,002-16,269,382 , GRCh38.p12 chr16|NT_187607.1: 531,831-1,927,385 LOC102724984, LOC728138, 50 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