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 96

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140843insertion1nstd232human GRCh37.p13 chr14: 22,136,548-22,136,548 , GRCh38.p12 chr14: 21,668,334-21,668,334 TRA, OR4E1
    nsv7072621inversion1nstd229human GRCh38 chr14: 20,991,576-21,885,954 , GRCh37.p13 chr14: 21,459,735-22,354,136 LINC00641, TRAV13-1, 61 more genes
    nsv6942779copy number variation1nstd229human GRCh38 chr14: 21,670,886-21,675,126 , GRCh37.p13 chr14: 22,139,101-22,143,341 TRA, OR4E1
    nsv6941845copy number variation1nstd229human GRCh38 chr14: 21,665,996-21,670,421 , GRCh37.p13 chr14: 22,134,210-22,138,636 OR4E1, OR4E2, 1 more genes
    nsv6637318copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,690,196-23,114,522 , GRCh38.p12 chr14: 20,222,037-22,645,313 TRAJ21, TRAJ44, 239 more genes
    nsv6486406copy number variation1nstd223human GRCh38 chr14: 21,538,051-22,772,225 , GRCh37.p13 chr14: 22,006,185-23,241,434 TRAJ54, TRAV9-1, 152 more genes
    nsv6481870copy number variation1nstd223human GRCh38 chr14: 21,667,201-21,668,000 , GRCh37.p13 chr14: 22,135,415-22,136,214 OR4E1, TRA
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 CDH24, KLHL33, 623 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 HNRNPC, FOXG1, 616 more genes
    nsv6290276copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 20,925,965-23,649,548 , GRCh38.p12 chr14: 20,457,806-23,180,339 ANG, APEX1, 255 more genes
    nsv6132583copy number variation1nstd213human GRCh37 chr14: 20,420,000-22,590,001 , GRCh38.p12 chr14: 19,951,841-22,122,043 HNRNPC, PNP, 157 more genes
    nsv6096419insertion1nstd212human GRCh38 chr14: 21,668,334-21,668,334 , GRCh37.p13 chr14: 22,136,548-22,136,548 TRA, OR4E1
    nsv5976625insertion1nstd209human GRCh38 chr14: 21,668,334-21,668,334 , GRCh37.p13 chr14: 22,136,548-22,136,548 TRA, OR4E1
    nsv5661165insertion1nstd207human GRCh38 chr14: 21,668,334-21,668,334 , GRCh37.p13 chr14: 22,136,548-22,136,548 OR4E1, TRA
    nsv5550513insertion1nstd206human GRCh38 chr14: 21,668,334-21,668,334 , GRCh37.p13 chr14: 22,136,548-22,136,548 TRA, OR4E1
    nsv5496298copy number variation1nstd206human GRCh38 chr14: 21,668,189-21,671,413 , GRCh37.p13 chr14: 22,136,403-22,139,628 TRA, OR4E1
    nsv4990769copy number variation1nstd200human GRCh38 chr14: 21,668,754-21,670,717 , GRCh37.p13 chr14: 22,136,967-22,138,932 OR4E1, TRA
    nsv4842081copy number variation1nstd200human GRCh37 chr14: 22,136,967-22,138,932 , GRCh38.p12 chr14: 21,668,754-21,670,717 TRA, OR4E1
    nsv4769153insertion1nstd186human GRCh37 chr14: 22,136,549-22,136,549 , GRCh38.p12 chr14: 21,668,335-21,668,335 TRA, OR4E1
    nsv4758385insertion1nstd199human GRCh37 chr14: 22,136,546-22,136,546 , GRCh38.p12 chr14: 21,668,332-21,668,332 TRA, OR4E1
    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