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 967

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5906416copy number variation1nstd209human GRCh38 chr4: 714,918-716,256 , GRCh37.p13 chr4: 708,707-710,045 PCGF3
    nsv5906309copy number variation1nstd209human GRCh38 chr4: 707,475-708,084 , GRCh37.p13 chr4: 701,264-701,873 PCGF3
    nsv5901659copy number variation1nstd209human GRCh38 chr4: 715,146-716,295 , GRCh37.p13 chr4: 708,935-710,084 PCGF3
    nsv5896234copy number variation1nstd209human GRCh38 chr4: 721,729-721,780 , GRCh37.p13 chr4: 715,518-715,569 PCGF3
    nsv5896207copy number variation1nstd209human GRCh38 chr4: 758,842-759,832 , GRCh37.p13 chr4: 752,630-753,620 PCGF3
    nsv5895393copy number variation1nstd209human GRCh38 chr4: 758,439-759,891 , GRCh37.p13 chr4: 752,227-753,679 PCGF3
    nsv5891609copy number variation1nstd209human GRCh38 chr4: 758,659-759,950 , GRCh37.p13 chr4: 752,447-753,738 PCGF3
    nsv5688227mobile element insertion2nstd211human GRCh38 chr4: 727,749-727,749 , GRCh37.p13 chr4: 721,538-721,538 PCGF3
    nsv5673651copy number variation1nstd102humanPathogenic GRCh37 chr4: 493,125-998,181 , GRCh38.p12 chr4: 499,336-1,004,393 ATP5ME, PDE6B, 19 more genes
    nsv5673565copy number variation1nstd102humanUncertain significance GRCh38 chr4: 1-705,161 , GRCh37.p13 chr4|NW_004775427.1: 1-503,215 , GRCh37.p13 chr4: 10,001-507,004 ABCA11P, LOC105374377, 23 more genes
    nsv5623806insertion1nstd207human GRCh38 chr4: 715,857-715,857 , GRCh37.p13 chr4: 709,646-709,646 PCGF3
    nsv5623431insertion1nstd207human GRCh38 chr4: 759,781-759,781 , GRCh37.p13 chr4: 753,569-753,569 PCGF3
    nsv5623004insertion1nstd207human GRCh38 chr4: 715,035-715,035 , GRCh37.p13 chr4: 708,824-708,824 PCGF3
    nsv5621683insertion1nstd207human GRCh38 chr4: 747,687-747,687 , GRCh37.p13 chr4: 741,475-741,475 PCGF3
    nsv5621006insertion1nstd207human GRCh38 chr4: 727,735-727,735 , GRCh37.p13 chr4: 721,524-721,524 PCGF3
    nsv5620606insertion1nstd207human GRCh38 chr4: 759,231-759,231 , GRCh37.p13 chr4: 753,019-753,019 PCGF3
    nsv5618347insertion1nstd207human GRCh38 chr4: 707,567-707,567 , GRCh37.p13 chr4: 701,356-701,356 PCGF3
    nsv5616842insertion1nstd207human GRCh38 chr4: 759,821-759,821 , GRCh37.p13 chr4: 753,609-753,609 PCGF3
    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