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 134

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148126copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,851,693-22,089,506 , GRCh38.p12 chr14: 21,383,534-21,621,353 OR10G3, SNORD9, 17 more genes
    nsv7094421copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,671,278-22,005,055 , GRCh38.p12 chr14: 21,203,119-21,536,921 RN7SL650P, SNORD9, 14 more genes
    nsv7094244copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,915,399-22,005,055 , GRCh38.p12 chr14: 20,447,240-21,536,921 ARHGEF40, LOC105370398, 78 more genes
    nsv7072621inversion1nstd229human GRCh38 chr14: 20,991,576-21,885,954 , GRCh37.p13 chr14: 21,459,735-22,354,136 LINC00641, TRAV13-1, 61 more genes
    nsv6947409copy number variation1nstd229human GRCh38 chr14: 21,515,702-21,519,740 , GRCh37.p13 chr14: 21,983,855-21,987,891 SALL2
    nsv6946491copy number variation1nstd229human GRCh38 chr14: 21,532,701-21,535,100 , GRCh37.p13 chr14: 22,000,835-22,003,234 SALL2
    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
    nsv6480182copy number variation1nstd223human GRCh38 chr14: 21,530,214-21,531,575 , GRCh37.p13 chr14: 21,998,348-21,999,709 SALL2
    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
    nsv5672730copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,756,136-22,005,055 , GRCh38.p12 chr14: 21,287,977-21,536,921 RAB2B, METTL3, 12 more genes
    nsv5508784copy number variation1nstd206human GRCh38 chr14: 21,527,990-21,535,163 , GRCh37.p13 chr14: 21,996,124-22,003,297 SALL2
    nsv5506506copy number variation1nstd206human GRCh38 chr14: 21,455,390-21,561,947 , GRCh37.p13 chr14: 21,923,549-22,030,078 SALL2, TOX4, 4 more genes
    nsv5495428copy number variation1nstd206human GRCh38 chr14: 21,530,484-21,531,605 , GRCh37.p13 chr14: 21,998,618-21,999,739 SALL2
    nsv5158550mobile element insertion1nstd203human GRCh38 chr14: 21,531,766-21,531,769 , GRCh37.p13 chr14: 21,999,900-21,999,903 SALL2
    nsv5156397mobile element insertion1nstd203human GRCh38 chr14: 21,531,756-21,531,769 , GRCh37.p13 chr14: 21,999,890-21,999,903 SALL2
    nsv5151286mobile element insertion1nstd203human GRCh38 chr14: 21,531,765-21,531,765 , GRCh37.p13 chr14: 21,999,899-21,999,899 SALL2
    nsv5149100mobile element insertion1nstd203human GRCh38 chr14: 21,531,724-21,531,765 , GRCh37.p13 chr14: 21,999,858-21,999,899 SALL2
    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