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 795

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120515copy number variation1nstd186human GRCh37 chr4: 1,086,777-1,086,827 , GRCh38.p12 chr4: 1,092,989-1,093,039 RNF212
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5905581copy number variation1nstd209human GRCh38 chr4: 1,054,425-1,054,716 , GRCh37.p13 chr4: 1,048,213-1,048,504 RNF212
    nsv5904328copy number variation1nstd209human GRCh38 chr4: 1,054,680-1,054,785 , GRCh37.p13 chr4: 1,048,468-1,048,573 RNF212
    nsv5903805copy number variation1nstd209human GRCh38 chr4: 1,078,999-1,079,273 , GRCh37.p13 chr4: 1,072,787-1,073,061 RNF212
    nsv5903042copy number variation1nstd209human GRCh38 chr4: 1,054,713-1,055,233 , GRCh37.p13 chr4: 1,048,501-1,049,021 RNF212
    nsv5901753copy number variation1nstd209human GRCh38 chr4: 1,053,964-1,054,384 , GRCh37.p13 chr4: 1,047,752-1,048,172 RNF212
    nsv5900221copy number variation1nstd209human GRCh38 chr4: 1,095,147-1,096,361 , GRCh37.p13 chr4: 1,088,935-1,090,149 RNF212
    nsv5898163copy number variation1nstd209human GRCh38 chr4: 1,054,949-1,055,283 , GRCh37.p13 chr4: 1,048,737-1,049,071 RNF212
    nsv5898057copy number variation1nstd209human GRCh38 chr4: 1,078,846-1,078,922 , GRCh37.p13 chr4: 1,072,634-1,072,710 RNF212
    nsv5897261copy number variation1nstd209human GRCh38 chr4: 1,065,732-1,066,018 , GRCh37.p13 chr4: 1,059,520-1,059,806 RNF212
    nsv5896883copy number variation1nstd209human GRCh38 chr4: 1,092,989-1,093,038 , GRCh37.p13 chr4: 1,086,777-1,086,826 RNF212
    nsv5895884copy number variation1nstd209human GRCh38 chr4: 1,069,993-1,070,626 , GRCh37.p13 chr4: 1,063,781-1,064,414 RNF212
    nsv5893871copy number variation1nstd209human GRCh38 chr4: 1,075,223-1,075,955 , GRCh37.p13 chr4: 1,069,011-1,069,743 RNF212
    nsv5892824copy number variation1nstd209human GRCh38 chr4: 1,095,143-1,096,576 , GRCh37.p13 chr4: 1,088,931-1,090,364 RNF212
    nsv5888368copy number variation1nstd209human GRCh38 chr4: 1,058,242-1,058,305 , GRCh37.p13 chr4: 1,052,030-1,052,093 RNF212
    nsv5620865insertion1nstd207human GRCh38 chr4: 1,054,692-1,054,692 , GRCh37.p13 chr4: 1,048,480-1,048,480 RNF212
    nsv5614273insertion2nstd207human GRCh38 chr4: 1,095,984-1,095,984 , GRCh37.p13 chr4: 1,089,772-1,089,772 RNF212
    nsv5609205insertion1nstd207human GRCh38 chr4: 1,058,312-1,058,312 , GRCh37.p13 chr4: 1,052,100-1,052,100 RNF212
    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