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 235

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6113588mobile element insertion1nstd186human GRCh37 chr15: 89,871,267-89,871,318 , GRCh38.p12 chr15: 89,328,036-89,328,087 POLG
    nsv5947393copy number variation1nstd209human GRCh38 chr15: 89,315,512-89,315,591 , GRCh37.p13 chr15: 89,858,743-89,858,822 POLG, FANCI
    nsv5929051copy number variation1nstd209human GRCh38 chr15: 89,325,034-89,325,231 , GRCh37.p13 chr15: 89,868,265-89,868,462 MIR6766, POLG
    nsv5711532mobile element insertion1nstd211human GRCh38 chr15: 89,318,172-89,318,172 , GRCh37.p13 chr15: 89,861,403-89,861,403 POLG
    nsv5710862mobile element insertion2nstd211human GRCh38 chr15: 89,328,036-89,328,036 , GRCh37.p13 chr15: 89,871,267-89,871,267 POLG
    nsv5672828copy number variation1nstd102humanPathogenic GRCh37 chr15: 89,790,873-89,876,991 , GRCh38.p12 chr15: 89,247,642-89,333,760 POLG, TRR-TCG1-1, 2 more genes
    nsv5672673copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 89,843,021-89,860,052 , GRCh38.p12 chr15: 89,299,790-89,316,821 POLG, FANCI
    nsv5663654insertion1nstd207human GRCh38 chr15: 89,325,195-89,325,195 , GRCh37.p13 chr15: 89,868,426-89,868,426 MIR6766, POLG
    nsv5659584insertion1nstd207human GRCh38 chr15: 89,325,073-89,325,073 , GRCh37.p13 chr15: 89,868,304-89,868,304 POLG, MIR6766
    nsv5657779insertion1nstd207human GRCh38 chr15: 89,315,541-89,315,541 , GRCh37.p13 chr15: 89,858,772-89,858,772 POLG, FANCI
    nsv5656917insertion1nstd207human GRCh38 chr15: 89,325,273-89,325,273 , GRCh37.p13 chr15: 89,868,504-89,868,504 MIR6766, POLG
    nsv5650002insertion1nstd207human GRCh38 chr15: 89,328,021-89,328,021 , GRCh37.p13 chr15: 89,871,252-89,871,252 POLG
    nsv5597244copy number variation1nstd207human GRCh38 chr15: 89,325,041-89,325,110 , GRCh37.p13 chr15: 89,868,272-89,868,341 POLG, MIR6766
    nsv5588393copy number variation1nstd207human GRCh38 chr15: 89,325,087-89,325,270 , GRCh37.p13 chr15: 89,868,318-89,868,501 POLG, MIR6766
    nsv5516950copy number variation1nstd206human GRCh38 chr15: 89,315,512-89,315,593 , GRCh37.p13 chr15: 89,858,743-89,858,824 POLG, FANCI
    nsv5424352mobile element insertion1nstd206human GRCh38 chr15: 89,328,036-89,328,087 , GRCh37.p13 chr15: 89,871,267-89,871,318 POLG
    nsv5414772mobile element insertion1nstd206human GRCh38 chr15: 89,318,172-89,318,223 , GRCh37.p13 chr15: 89,861,403-89,861,454 POLG
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5300841copy number variation1nstd204human GRCh37.p13 chr15: 89,868,257-89,868,511 , GRCh38.p13 chr15: 89,325,026-89,325,280 POLG, MIR6766
    nsv5155990mobile element insertion1nstd203human GRCh38 chr15: 89,328,020-89,328,036 , GRCh37.p13 chr15: 89,871,251-89,871,267 POLG
    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