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Items: 1 to 20 of 333

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143279insertion1nstd232human GRCh37.p13 chr19: 5,996,263-5,996,263 , GRCh38.p12 chr19: 5,996,252-5,996,252 RFX2, RANBP3-DT
    nsv7068649inversion1nstd229human GRCh38 chr19: 4,313,135-7,007,201 , GRCh37.p13 chr19: 4,313,132-7,007,212 CAPS, SH2D3A, 93 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7067256inversion1nstd229human GRCh38 chr19: 5,932,247-6,023,614 , GRCh37.p13 chr19: 5,932,258-6,023,625 RFX2, RANBP3-DT, 1 more genes
    nsv7066921inversion1nstd229human GRCh38 chr19: 4,809,260-7,077,959 , GRCh37.p13 chr19: 4,809,272-7,077,970 MLLT1, GPR108, 74 more genes
    nsv7064589inversion1nstd229human GRCh38 chr19: 6,052,664-6,088,085 , GRCh37.p13 chr19: 6,052,675-6,088,096 LOC100128144, RFX2
    nsv7062457inversion1nstd229human GRCh38 chr19: 6,093,360-6,096,890 , GRCh37.p13 chr19: 6,093,371-6,096,901 RFX2
    nsv7059289inversion1nstd229human GRCh38 chr19: 5,886,502-5,991,855 , GRCh37.p13 chr19: 5,886,513-5,991,866 RANBP3, NDUFA11, 4 more genes
    nsv7017079copy number variation1nstd229human GRCh38 chr19: 6,013,544-6,018,027 , GRCh37.p13 chr19: 6,013,555-6,018,038 RANBP3-DT, RFX2
    nsv7016225copy number variation1nstd229human GRCh38 chr19: 6,021,300-6,025,457 , GRCh37.p13 chr19: 6,021,311-6,025,468 RFX2
    nsv7014345copy number variation1nstd229human GRCh38 chr19: 6,110,001-6,197,600 , GRCh37.p13 chr19: 6,110,012-6,197,611 LOC105372255, RFX2, 1 more genes
    nsv7012527copy number variation1nstd229human GRCh38 chr19: 6,089,316-6,099,436 , GRCh37.p13 chr19: 6,089,327-6,099,447 RFX2
    nsv7010716copy number variation1nstd229human GRCh38 chr19: 6,110,525-6,112,786 , GRCh37.p13 chr19: 6,110,536-6,112,797 RFX2
    nsv7010089copy number variation1nstd229human GRCh38 chr19: 6,032,601-6,042,100 , GRCh37.p13 chr19: 6,032,612-6,042,111 RFX2
    nsv7006866copy number variation1nstd229human GRCh38 chr19: 6,059,922-6,077,389 , GRCh37.p13 chr19: 6,059,933-6,077,400 RFX2, LOC100128144
    nsv7006589copy number variation1nstd229human GRCh38 chr19: 6,109,480-6,109,549 , GRCh37.p13 chr19: 6,109,491-6,109,560 RFX2
    nsv7005780copy number variation1nstd229human GRCh38 chr19: 6,025,137-6,025,553 , GRCh37.p13 chr19: 6,025,148-6,025,564 RFX2
    nsv7004343copy number variation1nstd229human GRCh38 chr19: 6,106,436-6,116,029 , GRCh37.p13 chr19: 6,106,447-6,116,040 RFX2
    nsv7002095copy number variation1nstd229human GRCh38 chr19: 5,998,256-6,062,144 , GRCh37.p13 chr19: 5,998,267-6,062,155 RANBP3-DT, RFX2
    nsv6998683copy number variation1nstd229human GRCh38 chr19: 6,017,201-6,021,100 , GRCh37.p13 chr19: 6,017,212-6,021,111 RANBP3-DT, RFX2
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