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 94

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114272mobile element insertion1nstd186human GRCh37 chr20: 58,638,131-58,638,131 , GRCh38.p12 chr20: 60,063,076-60,063,076 LINC02910
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5977329insertion1nstd209human GRCh38 chr20: 60,063,076-60,063,076 , GRCh37.p13 chr20: 58,638,131-58,638,131 LINC02910
    nsv5953861copy number variation1nstd209human GRCh38 chr20: 60,052,096-60,064,483 , GRCh37.p13 chr20: 58,627,151-58,639,538 LINC02910
    nsv5884689copy number variation1nstd209human GRCh38 chr20: 60,052,452-60,063,540 , GRCh37.p13 chr20: 58,627,507-58,638,595 LINC02910
    nsv5880172copy number variation2nstd209human GRCh38 chr20: 60,053,327-60,055,155 , GRCh37.p13 chr20: 58,628,382-58,630,210 LINC02910
    nsv5874564copy number variation2nstd209human GRCh38 chr20: 60,055,693-60,060,478 , GRCh37.p13 chr20: 58,630,748-58,635,533 LINC02910
    nsv5700030mobile element insertion2nstd211human GRCh38 chr20: 60,063,097-60,063,097 , GRCh37.p13 chr20: 58,638,152-58,638,152 LINC02910
    nsv5599002copy number variation1nstd207human GRCh38 chr20: 60,064,119-60,064,185 , GRCh37.p13 chr20: 58,639,174-58,639,240 LINC02910
    nsv5514531copy number variation1nstd206human GRCh38 chr20: 60,055,124-60,055,491 , GRCh37.p13 chr20: 58,630,179-58,630,546 LINC02910
    nsv5430551mobile element insertion1nstd206human GRCh38 chr20: 60,063,076-60,063,076 , GRCh37.p13 chr20: 58,638,131-58,638,131 LINC02910
    nsv5177612mobile element insertion1nstd203human GRCh38 chr20: 60,063,076-60,063,097 , GRCh37.p13 chr20: 58,638,131-58,638,152 LINC02910
    nsv5170693mobile element insertion1nstd203human GRCh38 chr20: 60,072,101-60,072,113 , GRCh37.p13 chr20: 58,647,156-58,647,168 LINC02910
    nsv4724710insertion1nstd186human GRCh37 chr20: 58,638,131-58,638,131 , GRCh38.p12 chr20: 60,063,076-60,063,076 LINC02910
    nsv4676332copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636 BMP7, MIR298, 153 more genes
    nsv4676181copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,788,101-62,762,405 , GRCh38.p12 chr20: 58,213,045-64,131,052 LOC105372697, MIR647, 174 more genes
    nsv4626735copy number variation1nstd183human GRCh37 chr20: 58,646,846-58,655,849 , GRCh38.p12 chr20: 60,071,791-60,080,794 , LINC02910
    nsv4569220insertion1nstd166human GRCh37.p13 chr20: 58,638,131-58,638,131 , GRCh38.p12 chr20: 60,063,076-60,063,076 LINC02910
    nsv4433289copy number variation1nstd172human GRCh37.p13 chr20: 58,634,001-58,635,000 , GRCh38.p12 chr20: 60,058,946-60,059,945 LINC02910
    nsv4357849copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528 RBM38, LAMA5, 192 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