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Items: 1 to 20 of 267

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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
    nsv7139428insertion1nstd232human GRCh37.p13 chr14: 105,481,735-105,481,735 , GRCh38.p12 chr14: 105,015,398-105,015,398 CDCA4
    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
    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
    nsv7063921inversion1nstd229human GRCh38 chr14: 105,011,361-105,107,786 , GRCh37.p13 chr14: 105,477,698-105,574,123 CDCA4, GPR132, 1 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
    nsv6973607copy number variation1nstd229human GRCh38 chr14: 104,978,362-105,152,093 , GRCh37.p13 chr14: 105,444,699-105,618,430 CDCA4, AHNAK2, 5 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
    nsv6960796copy number variation1nstd229human GRCh38 chr14: 105,017,165-105,020,389 , GRCh37.p13 chr14: 105,483,502-105,486,726 CDCA4
    nsv6960718copy number variation1nstd229human GRCh38 chr14: 105,005,533-105,011,022 , GRCh37.p13 chr14: 105,471,870-105,477,359 CDCA4
    nsv6958323copy number variation1nstd229human GRCh38 chr14: 105,015,381-105,015,469 , GRCh37.p13 chr14: 105,481,718-105,481,806 CDCA4
    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
    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
    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
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