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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
    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
    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
    nsv7062669inversion1nstd229human GRCh38 chr14: 104,908,222-105,065,167 , GRCh37.p13 chr14: 105,374,559-105,531,504 PLD4, GPR132, 3 more genes
    nsv6970683copy number variation1nstd229human GRCh38 chr14: 104,920,101-105,102,900 , GRCh37.p13 chr14: 105,386,438-105,569,237 CLBA1, LINC02298, 4 more genes
    nsv6967591copy number variation1nstd229human GRCh38 chr14: 104,884,001-104,933,000 , GRCh37.p13 chr14: 105,350,338-105,399,337 PLD4, CEP170B
    nsv6966044copy number variation1nstd229human GRCh38 chr14: 104,914,238-104,971,977 , GRCh37.p13 chr14: 105,380,575-105,438,314 AHNAK2, PLD4
    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
    nsv6959986copy number variation1nstd229human GRCh38 chr14: 104,937,336-104,967,433 , GRCh37.p13 chr14: 105,403,673-105,433,770 AHNAK2, PLD4
    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
    nsv6622352copy number variation1nstd224human GRCh37 chr14: 105,391,005-105,408,341 , GRCh38.p12 chr14: 104,924,668-104,942,004 PLD4, AHNAK2
    nsv6622237copy number variation1nstd224human GRCh37 chr14: 105,391,005-105,410,471 , GRCh38.p12 chr14: 104,924,668-104,944,134 PLD4, AHNAK2
    nsv6508114copy number variation1nstd223human GRCh38 chr14: 104,918,223-105,014,225 , GRCh37.p13 chr14: 105,384,560-105,480,562 PLD4, AHNAK2, 2 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
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