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 255

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946119copy number variation1nstd209human GRCh38 chr12: 53,409,964-53,410,258 , GRCh37.p13 chr12: 53,803,748-53,804,042 SP1
    nsv5942842copy number variation1nstd209human GRCh38 chr12: 53,399,596-53,402,486 , GRCh37.p13 chr12: 53,793,380-53,796,270 SP1
    nsv5928761copy number variation1nstd209human GRCh38 chr12: 53,378,053-53,378,926 , GRCh37.p13 chr12: 53,771,837-53,772,710 SP1
    nsv5509214copy number variation1nstd206human GRCh38 chr12: 53,378,055-53,378,927 , GRCh37.p13 chr12: 53,771,839-53,772,711 SP1
    nsv5269754copy number variation1nstd204human GRCh38.p13 chr12: 53,319,601-53,446,000 , GRCh37.p13 chr12: 53,713,385-53,839,784 SP7, PRR13, 3 more genes
    nsv5266008copy number variation1nstd204human GRCh38.p13 chr12: 53,248,501-53,495,800 , GRCh37.p13 chr12: 53,642,285-53,889,584 PCBP2, AAAS, 11 more genes
    nsv5196162mobile element insertion1nstd203human GRCh38 chr12: 53,416,784-53,416,784 , GRCh37.p13 chr12: 53,810,568-53,810,568 SP1
    nsv5193789mobile element insertion1nstd203human GRCh38 chr12: 53,416,780-53,416,780 , GRCh37.p13 chr12: 53,810,564-53,810,564 SP1
    nsv5191724mobile element insertion1nstd203human GRCh38 chr12: 53,416,785-53,416,785 , GRCh37.p13 chr12: 53,810,569-53,810,569 SP1
    nsv5187259mobile element insertion1nstd203human GRCh38 chr12: 53,416,779-53,416,779 , GRCh37.p13 chr12: 53,810,563-53,810,563 SP1
    nsv5138623mobile element insertion1nstd203human GRCh38 chr12: 53,399,625-53,399,675 , GRCh37.p13 chr12: 53,793,409-53,793,459 SP1
    nsv5132593mobile element insertion1nstd203human GRCh38 chr12: 53,396,265-53,396,297 , GRCh37.p13 chr12: 53,790,049-53,790,081 SP1
    nsv5130617mobile element insertion1nstd203human GRCh38 chr12: 53,396,274-53,396,297 , GRCh37.p13 chr12: 53,790,058-53,790,081 SP1
    nsv5130437mobile element insertion1nstd203human GRCh38 chr12: 53,385,313-53,385,365 , GRCh37.p13 chr12: 53,779,097-53,779,149 SP1
    nsv5125059mobile element insertion1nstd203human GRCh38 chr12: 53,393,345-53,393,376 , GRCh37.p13 chr12: 53,787,129-53,787,160 SP1
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4972761copy number variation1nstd200human GRCh38 chr12: 53,401,052-53,402,481 , GRCh37.p13 chr12: 53,794,836-53,796,265 SP1
    nsv4972760copy number variation1nstd200human GRCh38 chr12: 53,393,810-53,398,466 , GRCh37.p13 chr12: 53,787,594-53,792,250 SP1
    nsv4972759copy number variation1nstd200human GRCh38 chr12: 53,378,055-53,378,927 , GRCh37.p13 chr12: 53,771,839-53,772,711 SP1
    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