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 363

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130221insertion1nstd186human GRCh37 chr15: 66,666,678-66,666,720 , GRCh38.p12 chr15: 66,374,340-66,374,382 TIPIN
    nsv6113978mobile element insertion1nstd186human GRCh37 chr15: 66,668,137-66,668,137 , GRCh38.p12 chr15: 66,375,799-66,375,799 TIPIN
    nsv5974835insertion1nstd209human GRCh38 chr15: 66,375,799-66,375,799 , GRCh37.p13 chr15: 66,668,137-66,668,137 TIPIN
    nsv5973660inversion1nstd209human GRCh38 chr15: 66,344,424-66,346,938 , GRCh37.p13 chr15: 66,636,762-66,639,276 TIPIN, SCARNA14
    nsv5946551copy number variation1nstd209human GRCh38 chr15: 66,380,151-66,380,288 , GRCh37.p13 chr15: 66,672,489-66,672,626 RPL9P25, TIPIN
    nsv5938215copy number variation1nstd209human GRCh38 chr15: 66,359,300-66,361,015 , GRCh37.p13 chr15: 66,651,638-66,653,353 TIPIN
    nsv5936088copy number variation1nstd209human GRCh38 chr15: 66,341,474-66,341,794 , GRCh37.p13 chr15: 66,633,812-66,634,132 TIPIN
    nsv5852390copy number variation1nstd209human GRCh38 chr15: 66,359,317-66,361,016 , GRCh37.p13 chr15: 66,651,655-66,653,354 TIPIN
    nsv5714934mobile element insertion1nstd211human GRCh38 chr15: 66,378,940-66,378,940 , GRCh37.p13 chr15: 66,671,278-66,671,278 RPL9P25, TIPIN
    nsv5707886mobile element insertion2nstd211human GRCh38 chr15: 66,374,340-66,374,340 , GRCh37.p13 chr15: 66,666,678-66,666,678 TIPIN
    nsv5703140mobile element insertion2nstd211human GRCh38 chr15: 66,375,813-66,375,813 , GRCh37.p13 chr15: 66,668,151-66,668,151 TIPIN
    nsv5655299insertion1nstd207human GRCh38 chr15: 66,375,799-66,375,799 , GRCh37.p13 chr15: 66,668,137-66,668,137 TIPIN
    nsv5647777insertion1nstd207human GRCh38 chr15: 66,374,331-66,374,331 , GRCh37.p13 chr15: 66,666,669-66,666,669 TIPIN
    nsv5594625copy number variation1nstd207human GRCh38 chr15: 66,341,474-66,341,794 , GRCh37.p13 chr15: 66,633,812-66,634,132 TIPIN
    nsv5551843insertion1nstd206human GRCh38 chr15: 66,374,340-66,374,382 , GRCh37.p13 chr15: 66,666,678-66,666,720 TIPIN
    nsv5515275copy number variation1nstd206human GRCh38 chr15: 66,341,486-66,341,795 , GRCh37.p13 chr15: 66,633,824-66,634,133 TIPIN
    nsv5515186copy number variation1nstd206human GRCh38 chr15: 66,381,862-66,384,711 , GRCh37.p13 chr15: 66,674,200-66,677,049 TIPIN
    nsv5415697mobile element insertion1nstd206human GRCh38 chr15: 66,375,799-66,375,799 , GRCh37.p13 chr15: 66,668,137-66,668,137 TIPIN
    nsv5383694mobile element deletion2nstd186human GRCh37 chr15: 66,633,824-66,634,133 , GRCh38.p12 chr15: 66,341,486-66,341,795 TIPIN
    nsv5380765copy number variation1nstd102humanUncertain significance GRCh37 chr15: 66,679,676-66,782,963 , GRCh38.p12 chr15: 66,387,338-66,490,625 MAP2K1, TIPIN, 3 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