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 501

    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
    nsv7137201copy number variation1nstd102humanPathogenic GRCh37 chr14: 103,636,647-107,285,437 , GRCh38.p12 chr14: 103,170,310-106,877,229 IGHD, IGH, 281 more genes
    nsv7094482copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,167,703-105,861,009 , GRCh38.p12 chr14: 104,701,366-105,394,672 AHNAK2, PLD4, 24 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
    nsv6967591copy number variation1nstd229human GRCh38 chr14: 104,884,001-104,933,000 , GRCh37.p13 chr14: 105,350,338-105,399,337 PLD4, CEP170B
    nsv6961308copy number variation1nstd229human GRCh38 chr14: 104,494,808-104,931,788 , GRCh37.p13 chr14: 104,961,145-105,398,125 LINC02280, SIVA1, 16 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
    nsv6496083copy number variation1nstd223human GRCh38 chr14: 104,890,049-104,890,871 , GRCh37.p13 chr14: 105,356,386-105,357,208 CEP170B
    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
    nsv6314860copy number variation1nstd102humanUncertain significance GRCh37 chr14: 103,336,539-105,861,009 , GRCh38.p12 chr14: 102,870,202-105,394,672 PLD4, AHNAK2, 80 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
    nsv6204244copy number variation1nstd214human GRCh38 chr14: 104,876,390-104,876,505 , GRCh37.p13 chr14: 105,342,727-105,342,842 CEP170B
    nsv6194866copy number variation1nstd214human GRCh38 chr14: 104,884,561-104,884,612 , GRCh37.p13 chr14: 105,350,898-105,350,949 CEP170B
    nsv6190804copy number variation1nstd214human GRCh38 chr14: 104,890,560-104,890,718 , GRCh37.p13 chr14: 105,356,897-105,357,055 CEP170B
    nsv6189034copy number variation1nstd214human GRCh38 chr14: 104,890,628-104,890,718 , GRCh37.p13 chr14: 105,356,965-105,357,055 CEP170B
    nsv6132861copy number variation1nstd213human GRCh37 chr14: 104,890,000-106,040,001 , GRCh38.p12 chr14: 104,423,663-105,573,664 AKT1, CRIP1, 40 more genes
    nsv6132582copy number variation1nstd213human GRCh37 chr14: 104,040,000-106,020,001 , GRCh38.p12 chr14: 103,573,663-105,533,002 PPP1R13B, GPR132, 57 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