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 141

    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
    nsv7059378inversion1nstd229human GRCh38 chr14: 87,626,566-93,230,083 , GRCh37.p13 chr14: 88,092,910-93,674,575 PSMC1, HISLA, 87 more genes
    nsv6968792copy number variation1nstd229human GRCh38 chr14: 93,169,201-93,215,200 , GRCh37.p13 chr14: 93,635,546-93,681,546 MOAP1, GON7, 2 more genes
    nsv6967099copy number variation1nstd229human GRCh38 chr14: 93,221,343-93,221,377 , GRCh37.p13 chr14: 93,687,689-93,687,723 UBR7
    nsv6964194copy number variation1nstd229human GRCh38 chr14: 92,932,640-93,474,765 , GRCh37.p13 chr14: 93,398,985-93,941,111 UNC79, UBR7, 12 more genes
    nsv6960578copy number variation1nstd229human GRCh38 chr14: 93,222,496-93,226,400 , GRCh37.p13 chr14: 93,688,842-93,692,746 UBR7, RPL18AP1
    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
    nsv6593924inversion1nstd223human GRCh38 chr14: 93,215,537-93,216,667 , GRCh37.p13 chr14: 93,681,883-93,683,013 UBR7
    nsv6592963inversion1nstd223human GRCh38 chr14: 86,486,184-95,139,000 , GRCh37.p13 chr14: 86,952,528-95,605,337 CCDC88C-DT, RPSAP4, 134 more genes
    nsv6592124inversion1nstd223human GRCh38 chr14: 93,205,509-93,206,129 , GRCh37.p13 chr14: 93,671,854-93,672,474 GON7, UBR7
    nsv6591551inversion1nstd223human GRCh38 chr14: 91,074,052-93,300,799 , GRCh37.p13 chr14: 91,540,396-93,674,575 LINC02287, LGMN, 39 more genes
    nsv6588196inversion1nstd223human GRCh38 chr14: 93,217,246-93,217,981 , GRCh37.p13 chr14: 93,683,592-93,684,327 UBR7
    nsv6576886inversion1nstd223human GRCh38 chr14: 87,626,564-93,230,084 , GRCh37.p13 chr14: 88,092,908-93,674,575 ATXN3, RIN3, 87 more genes
    nsv6509985copy number variation1nstd223human GRCh38 chr14: 93,228,459-93,230,463 , GRCh37.p13 chr14: 93,694,805-93,696,809 UBR7
    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
    nsv6309604copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 93,687,728-95,560,403 , GRCh38.p12 chr14: 93,638,887-95,094,066 , GRCh38.p12 chr14|NT_187601.1: 335,944-1,475,710 SERPINA3, SERPINA6, 43 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