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 349

    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
    nsv7074872inversion1nstd229human GRCh38 chr14: 93,271,258-93,271,300 , GRCh37.p13 chr14: 93,737,604-93,737,646 BTBD7
    nsv6976330copy number variation1nstd229human GRCh38 chr14: 93,273,319-93,273,520 , GRCh37.p13 chr14: 93,739,665-93,739,866 BTBD7
    nsv6975476copy number variation1nstd229human GRCh38 chr14: 93,232,467-93,235,875 , GRCh37.p13 chr14: 93,698,813-93,702,221 BTBD7
    nsv6971574copy number variation1nstd229human GRCh38 chr14: 93,313,501-93,315,800 , GRCh37.p13 chr14: 93,779,847-93,782,146 BTBD7
    nsv6971077copy number variation1nstd229human GRCh38 chr14: 93,251,701-93,272,900 , GRCh37.p13 chr14: 93,718,047-93,739,246 BTBD7
    nsv6966337copy number variation1nstd229human GRCh38 chr14: 93,290,501-93,292,800 , GRCh37.p13 chr14: 93,756,847-93,759,146 BTBD7
    nsv6965609copy number variation1nstd229human GRCh38 chr14: 93,266,487-93,266,528 , GRCh37.p13 chr14: 93,732,833-93,732,874 BTBD7
    nsv6965346copy number variation1nstd229human GRCh38 chr14: 93,306,149-93,307,110 , GRCh37.p13 chr14: 93,772,495-93,773,456 BTBD7
    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
    nsv6960910copy number variation1nstd229human GRCh38 chr14: 93,270,464-93,277,374 , GRCh37.p13 chr14: 93,736,810-93,743,720 BTBD7
    nsv6960677copy number variation1nstd229human GRCh38 chr14: 93,328,561-93,331,624 , GRCh37.p13 chr14: 93,794,907-93,797,970 UNC79, BTBD7
    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
    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
    nsv6588568inversion1nstd223human GRCh38 chr14: 93,252,057-93,252,644 , GRCh37.p13 chr14: 93,718,403-93,718,990 BTBD7
    nsv6587900inversion1nstd223human GRCh38 chr14: 93,290,589-93,292,188 , GRCh37.p13 chr14: 93,756,935-93,758,534 BTBD7
    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