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Items: 1 to 20 of 424

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    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
    nsv7094420copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,452,081-105,644,072 , GRCh38.p12 chr14: 104,985,744-105,177,735 JAG2, GPR132, 5 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
    nsv7073984inversion1nstd229human GRCh38 chr14: 105,171,356-105,177,843 , GRCh37.p13 chr14: 105,637,693-105,644,180 NUDT14
    nsv7071453inversion1nstd229human GRCh38 chr14: 104,922,043-106,758,290 , GRCh37.p13 chr14: 105,388,380-106,929,356 , GRCh37.p13 chr14|NW_004166863.1: 1-1,421,457 IGHD1-14, IGHVII-53-1, 206 more genes
    nsv7068446inversion1nstd229human GRCh38 chr14: 105,177,031-105,181,314 , GRCh37.p13 chr14: 105,643,368-105,647,651 NUDT14
    nsv6960814copy number variation1nstd229human GRCh38 chr14: 105,137,201-105,318,400 , GRCh37.p13 chr14: 105,603,538-105,784,737 BRF1, JAG2, 4 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
    nsv6635550copy number variation1nstd227human GRCh38.p12 chr14: 105,150,705-105,209,364 , GRCh37 chr14: 105,617,042-105,675,701 BRF1, JAG2, 2 more genes
    nsv6622353copy number variation1nstd224human GRCh37 chr14: 105,452,770-105,695,249 , GRCh38.p12 chr14: 104,986,433-105,228,912 BRF1, JAG2, 6 more genes
    nsv6507494copy number variation1nstd223human GRCh38 chr14: 105,160,601-105,186,200 , GRCh37.p13 chr14: 105,626,938-105,652,537 JAG2, NUDT14
    nsv6497432copy number variation1nstd223human GRCh38 chr14: 105,136,201-105,186,300 , GRCh37.p13 chr14: 105,602,538-105,652,637 NUDT14, MIR6765, 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
    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
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