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 202

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148227copy number variation1nstd102humanPathogenic GRCh38 chr14: 102,263,440-106,874,929 , GRCh37.p13 chr14: 102,729,777-107,283,138 TNFAIP2, IGHV4-30-2, 306 more genes
    nsv7094241copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,442,029-105,861,009 , GRCh38.p12 chr14: 101,975,692-105,394,672 LOC107984670, MARK3, 101 more genes
    nsv7094007copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,228,231-105,861,009 , GRCh38.p12 chr14: 101,761,894-105,394,672 CLBA1, BAG5, 105 more genes
    nsv6970176copy number variation1nstd229human GRCh38 chr14: 102,316,874-102,383,598 , GRCh37.p13 chr14: 102,783,211-102,849,935 TRI-AAT5-4, TECPR2, 2 more genes
    nsv6969794copy number variation1nstd229human GRCh38 chr14: 102,207,096-102,319,544 , GRCh37.p13 chr14: 102,673,433-102,785,881 TRI-AAT5-4, WDR20, 2 more genes
    nsv6969186copy number variation1nstd229human GRCh38 chr14: 102,302,577-102,330,429 , GRCh37.p13 chr14: 102,768,914-102,796,766 TRI-AAT5-4, ZNF839, 1 more genes
    nsv6963986copy number variation1nstd229human GRCh38 chr14: 102,304,701-102,348,800 , GRCh37.p13 chr14: 102,771,038-102,815,137 TRI-AAT5-4, CINP, 2 more genes
    nsv6962550copy number variation1nstd229human GRCh38 chr14: 102,336,413-102,351,250 , GRCh37.p13 chr14: 102,802,750-102,817,587 CINP, ZNF839
    nsv6960497copy number variation1nstd229human GRCh38 chr14: 102,155,025-102,356,399 , GRCh37.p13 chr14: 102,621,362-102,822,736 WDR20, ZNF839, 4 more genes
    nsv6959347copy number variation1nstd229human GRCh38 chr14: 102,147,957-102,398,368 , GRCh37.p13 chr14: 102,614,294-102,864,705 TRI-AAT5-4, LOC105370677, 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
    nsv6583670inversion1nstd223human GRCh38 chr14: 102,324,646-102,325,553 , GRCh37.p13 chr14: 102,790,983-102,791,890 ZNF839
    nsv6512816copy number variation1nstd223human GRCh38 chr14: 102,272,410-102,317,140 , GRCh37.p13 chr14: 102,738,747-102,783,477 ZNF839, MOK, 1 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
    nsv6314048copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,732,158-107,285,437 , GRCh38.p12 chr14: 101,265,821-106,877,229 IGHD4-23, XRCC3, 329 more genes
    nsv6309344copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,229,222-105,861,009 , GRCh38.p12 chr14: 101,762,885-105,394,672 LOC107984648, RN7SL634P, 105 more genes
    nsv6291499copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,593,860-106,160,500 , GRCh38.p12 chr14: 101,127,523-105,605,042 CDC42BPB, COA8, 133 more genes
    nsv6035618copy number variation1nstd212human GRCh38 chr14: 102,340,042-102,340,341 , GRCh37.p13 chr14: 102,806,379-102,806,678 ZNF839
    nsv5973101insertion1nstd209human GRCh38 chr14: 102,328,370-102,328,370 , GRCh37.p13 chr14: 102,794,707-102,794,707 ZNF839
    nsv5713735mobile element insertion1nstd211human GRCh38 chr14: 102,316,317-102,316,317 , GRCh37.p13 chr14: 102,782,654-102,782,654 TRI-AAT5-4, ZNF839
    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