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Items: 1 to 20 of 180

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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
    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
    nsv7062190inversion1nstd229human GRCh38 chr14: 103,555,287-104,539,425 , GRCh37.p13 chr14: 104,021,624-104,966,919 RNU4-68P, MIR203B, 21 more genes
    nsv6977817copy number variation1nstd229human GRCh38 chr14: 103,673,601-103,934,800 , GRCh37.p13 chr14: 104,139,938-104,401,137 ZFYVE21, XRCC3, 7 more genes
    nsv6977791copy number variation1nstd229human GRCh38 chr14: 103,907,805-103,913,302 , GRCh37.p13 chr14: 104,374,142-104,379,639 ATP5MJ
    nsv6968087copy number variation1nstd229human GRCh38 chr14: 103,909,601-103,919,000 , GRCh37.p13 chr14: 104,375,938-104,385,337 ATP5MJ
    nsv6961327copy number variation1nstd229human GRCh38 chr14: 103,914,501-103,921,100 , GRCh37.p13 chr14: 104,380,838-104,387,437 ATP5MJ
    nsv6958871copy number variation1nstd229human GRCh38 chr14: 103,914,992-103,915,173 , GRCh37.p13 chr14: 104,381,329-104,381,510 ATP5MJ
    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
    nsv6586128inversion1nstd223human GRCh38 chr14: 103,918,506-103,918,954 , GRCh37.p13 chr14: 104,384,843-104,385,291 ATP5MJ
    nsv6510684copy number variation1nstd223human GRCh38 chr14: 103,915,503-103,916,604 , GRCh37.p13 chr14: 104,381,840-104,382,941 ATP5MJ
    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
    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
    nsv6027767copy number variation1nstd212human GRCh38 chr14: 103,918,430-103,918,534 , GRCh37.p13 chr14: 104,384,767-104,384,871 ATP5MJ
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