Assay Details
Target Gene Details
Entrez Gene ID: | 6929 |
Gene Name: | transcription factor 3 |
Gene Aliases: |
AGM8, E2A, E47, ITF1, TCF-3, VDIR, bHLHb21 |
Location: |
Chr.19:1609290-1652590 on Build GRCh38 |
Assay Gene Location: | Within Intron 13 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv32942 | Chr.19:1320268 - 1999205 on Build GRCh38 | Gain+Loss | GAMT ADAMTSL5 SCAMP4 C19orf25 ADAT3 DAZAP1 RPS15 CSNK1G2 UQCR11 MIR1909 NDUFS7 ABHD17A APC2 TCF3 MBD3 MUM1 MEX3D REEP6 ONECUT3 ATP8B3 CSNK1G2-AS1 REXO1 BTBD2 PCSK4 PLK5 LOC100288123 KLF16 |
nsv953942 | Chr.19:1371602 - 2057401 on Build GRCh38 | Deletion | GAMT ADAMTSL5 SCAMP4 C19orf25 ADAT3 MKNK2 DAZAP1 RPS15 CSNK1G2 UQCR11 MIR1909 NDUFS7 ABHD17A APC2 TCF3 MBD3 MUM1 MEX3D REEP6 ONECUT3 ATP8B3 CSNK1G2-AS1 REXO1 BTBD2 PCSK4 PLK5 LOC100288123 KLF16 |
More Information
Additional Information:
For this assay, SNP(s) [rs72989730] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |