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 122

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5939572copy number variation1nstd209human GRCh38 chr14: 70,813,501-70,813,628 , GRCh37.p13 chr14: 71,280,218-71,280,345 MAP3K9-DT
    nsv5652155insertion1nstd207human GRCh38 chr14: 70,813,501-70,813,501 , GRCh37.p13 chr14: 71,280,218-71,280,218 MAP3K9-DT
    nsv5503842copy number variation1nstd206human GRCh38 chr14: 70,813,492-70,813,637 , GRCh37.p13 chr14: 71,280,209-71,280,354 MAP3K9-DT
    nsv5390679copy number variation3nstd186human GRCh37 chr14: 71,280,209-71,280,354 , GRCh38.p12 chr14: 70,813,492-70,813,637 MAP3K9-DT
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5004751copy number variation1nstd200human GRCh38 chr14: 70,813,492-70,813,637 , GRCh37.p13 chr14: 71,280,209-71,280,354 MAP3K9-DT
    nsv5004749copy number variation1nstd200human GRCh38 chr14: 70,762,287-71,042,561 , GRCh37.p13 chr14: 71,229,004-71,509,278 MAP3K9, GTF3AP2, 4 more genes
    nsv5004748copy number variation1nstd200human GRCh38 chr14: 70,675,354-70,999,301 , GRCh37.p13 chr14: 71,142,071-71,466,018 LINC01269, MAP3K9, 5 more genes
    nsv4839282copy number variation1nstd200human GRCh37 chr14: 71,280,209-71,280,354 , GRCh38.p12 chr14: 70,813,492-70,813,637 MAP3K9-DT
    nsv4625727copy number variation1nstd183human GRCh37 chr14: 71,269,111-71,667,692 , GRCh38.p12 chr14: 70,802,394-71,200,975 , MAP3K9, 7 more genes
    nsv4573243mobile element insertion1nstd166human GRCh37.p13 chr14: 71,283,909-71,283,909 , GRCh38.p12 chr14: 70,817,192-70,817,192 MAP3K9-DT
    nsv4457158copy number variation1nstd102humanUncertain significance GRCh37 chr14: 71,206,597-71,690,700 , GRCh38.p12 chr14: 70,739,880-71,223,983 TMEM183AP4, MAP3K9-DT, 6 more genes
    nsv4445402insertion1nstd175human GRCh37 chr14: 71,280,209-71,280,209 , GRCh38.p12 chr14: 70,813,492-70,813,492 MAP3K9-DT
    nsv4217082copy number variation1nstd166human GRCh37.p13 chr14: 71,258,890-71,572,556 , GRCh38.p12 chr14: 70,792,173-71,105,839 MAP3K9, PCNX1, 5 more genes
    nsv3948027insertion1nstd167human GRCh37 chr14: 71,280,218-71,280,218 , GRCh38.p12 chr14: 70,813,501-70,813,501 MAP3K9-DT
    nsv3923727copy number variation1nstd102humanPathogenic GRCh37 chr14: 70,028,816-82,441,728 , GRCh38 chr14: 69,562,099-81,975,384 , NCBI36 chr14: 69,098,569-81,511,481 CEP128, COX6CP11, 240 more genes
    nsv3922873copy number variation1nstd102humanUncertain significance GRCh37 chr14: 71,219,177-72,957,401 , NCBI36 chr14: 70,288,930-72,027,154 , GRCh38 chr14: 70,752,460-72,490,693 LOC105370559, MAP3K9-DT, 15 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SRMP2, IGHV3-71, 1929 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 MIR656, TRAJ59, 1918 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