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 93

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137135copy number variation1nstd102humanPathogenic GRCh37 chr14: 88,401,076-94,725,706 , GRCh38.p12 chr14: 87,934,732-94,140,555 LOC100128939, FAM181A-AS1, 104 more genes
    nsv7094351copy number variation1nstd102humanUncertain significance GRCh37 chr14: 90,429,459-97,347,545 , GRCh38.p12 chr14: 89,963,115-96,881,208 FBLN5, CYB5AP3, 135 more genes
    nsv7094350copy number variation1nstd102humanUncertain significance GRCh37 chr14: 90,429,459-94,856,914 , GRCh38.p12 chr14: 89,963,115-94,390,577 LOC105370619, SLC24A4, 78 more genes
    nsv7061728inversion1nstd229human GRCh38 chr14: 91,125,236-91,125,303 , GRCh37.p13 chr14: 91,591,580-91,591,647 DGLUCY, SNORA11B
    nsv7059378inversion1nstd229human GRCh38 chr14: 87,626,566-93,230,083 , GRCh37.p13 chr14: 88,092,910-93,674,575 PSMC1, HISLA, 87 more genes
    nsv7058992inversion1nstd229human GRCh38 chr14: 90,104,468-93,174,563 , GRCh37.p13 chr14: 90,570,812-93,372,264 LINC02321, TC2N, 48 more genes
    nsv6972042copy number variation1nstd229human GRCh38 chr14: 91,125,101-91,129,100 , GRCh37.p13 chr14: 91,591,445-91,595,444 DGLUCY, SNORA11B
    nsv6970110copy number variation1nstd229human GRCh38 chr14: 91,115,971-91,229,377 , GRCh37.p13 chr14: 91,582,315-91,695,721 DGLUCY, SNORA11B
    nsv6962058copy number variation1nstd229human GRCh38 chr14: 90,948,900-91,372,818 , GRCh37.p13 chr14: 91,415,244-91,839,162 RNU7-30P, GPR68, 5 more genes
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6637462copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 81,593,708-97,059,276 , GRCh38.p12 chr14: 81,127,364-96,592,939 SERPINA3, BDKRB1, 210 more genes
    nsv6637201copy number variation1nstd102humanUncertain significance GRCh37 chr14: 91,352,234-91,669,929 , GRCh38.p12 chr14: 90,885,890-91,203,585 DGLUCY, SNORA11B, 2 more genes
    nsv6622803copy number variation1nstd224human GRCh37 chr14: 91,593,301-91,690,796 , GRCh38.p12 chr14: 91,126,957-91,224,452 DGLUCY, SNORA11B
    nsv6592963inversion1nstd223human GRCh38 chr14: 86,486,184-95,139,000 , GRCh37.p13 chr14: 86,952,528-95,605,337 CCDC88C-DT, RPSAP4, 134 more genes
    nsv6591551inversion1nstd223human GRCh38 chr14: 91,074,052-93,300,799 , GRCh37.p13 chr14: 91,540,396-93,674,575 LINC02287, LGMN, 39 more genes
    nsv6576886inversion1nstd223human GRCh38 chr14: 87,626,564-93,230,084 , GRCh37.p13 chr14: 88,092,908-93,674,575 ATXN3, RIN3, 87 more genes
    nsv6511480copy number variation1nstd223human GRCh38 chr14: 90,948,900-91,372,817 , GRCh37.p13 chr14: 91,415,244-91,839,161 GPR68, RPS6KA5, 5 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6314190copy number variation1nstd102humanPathogenic GRCh37 chr14: 88,345,625-94,773,741 , GRCh38.p12 chr14: 87,879,281-94,140,555 EML5, LOC105370612, 104 more genes
    nsv6133140copy number variation1nstd213human GRCh37 chr14: 90,990,000-93,500,001 , GRCh38.p12 chr14: 90,523,656-92,905,919 ATXN3, GPR68, 34 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