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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148135copy number variation1nstd102humanUncertain significance GRCh37 chr14: 57,675,327-59,806,898 , GRCh38.p12 chr14: 57,208,609-59,340,180 HMGB1P14, TOMM20L-DT, 36 more genes
    nsv7139643copy number variation1nstd232human GRCh37.p13 chr14: 58,724,564-58,724,641 , GRCh38.p12 chr14: 58,257,846-58,257,923 PSMA3
    nsv7094257copy number variation1nstd102humanUncertain significance GRCh37 chr14: 58,711,639-58,718,980 , GRCh38.p12 chr14: 58,244,921-58,252,262 PSMA3
    nsv7069510inversion1nstd229human GRCh38 chr14: 57,948,807-58,720,869 , GRCh37.p13 chr14: 58,415,525-59,187,587 RN7SL598P, TRK-CTT1-1, 19 more genes
    nsv7060499inversion1nstd229human GRCh38 chr14: 57,927,850-58,665,319 , GRCh37.p13 chr14: 58,394,568-59,132,037 TOMM20L, KIAA0586, 19 more genes
    nsv7060471inversion1nstd229human GRCh38 chr14: 54,671,401-63,742,041 , GRCh37.p13 chr14: 55,138,119-64,208,759 KTN1, OTX2-AS1, 153 more genes
    nsv6952443copy number variation1nstd229human GRCh38 chr14: 57,104,906-61,096,631 , GRCh37.p13 chr14: 57,571,624-61,563,349 LRRC9, RTN1, 71 more genes
    nsv6949011copy number variation1nstd229human GRCh38 chr14: 57,104,849-61,096,728 , GRCh37.p13 chr14: 57,571,567-61,563,446 MAD2L1P1, AP5M1, 71 more genes
    nsv6945732copy number variation1nstd229human GRCh38 chr14: 58,178,001-58,257,600 , GRCh37.p13 chr14: 58,644,719-58,724,318 PSMA3, ACTR10, 2 more genes
    nsv6943620copy number variation1nstd229human GRCh38 chr14: 58,109,804-58,253,257 , GRCh37.p13 chr14: 58,576,522-58,719,975 PSMA3, ACTR10, 4 more genes
    nsv6941530copy number variation1nstd229human GRCh38 chr14: 58,267,048-58,267,222 , GRCh37.p13 chr14: 58,733,766-58,733,940 PSMA3, PSMA3-AS1
    nsv6940596copy number variation1nstd229human GRCh38 chr14: 58,257,715-58,258,073 , GRCh37.p13 chr14: 58,724,433-58,724,791 PSMA3
    nsv6940376copy number variation1nstd229human GRCh38 chr14: 58,224,718-58,257,255 , GRCh37.p13 chr14: 58,691,436-58,723,973 ACTR10, PSMA3, 1 more genes
    nsv6637682copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 57,804,997-63,590,203 , GRCh38.p12 chr14: 57,338,279-63,123,485 PARP1P2, HIF1A, 91 more genes
    nsv6622787copy number variation1nstd224human GRCh37 chr14: 57,287,812-59,826,703 , GRCh38.p12 chr14: 56,821,094-59,359,985 KIAA0586, DAAM1, 41 more genes
    nsv6595156inversion1nstd223human GRCh38 chr14: 58,256,433-58,257,118 , GRCh37.p13 chr14: 58,723,151-58,723,836 PSMA3
    nsv6594267inversion1nstd223human GRCh38 chr14: 54,883,431-63,921,497 , GRCh37.p13 chr14: 55,350,149-64,388,215 RPL36AP1, GNRHR2P1, 152 more genes
    nsv6593078inversion1nstd223human GRCh38 chr14: 58,255,483-58,256,158 , GRCh37.p13 chr14: 58,722,201-58,722,876 PSMA3
    nsv6591226inversion1nstd223human GRCh38 chr14: 58,248,708-58,249,081 , GRCh37.p13 chr14: 58,715,426-58,715,799 PSMA3
    nsv6591060inversion1nstd223human GRCh38 chr14: 58,249,737-58,250,043 , GRCh37.p13 chr14: 58,716,455-58,716,761 PSMA3
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