Genomic Map
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Target Gene Details
Entrez Gene ID: | 441094 |
Gene Name: | NR2F1 antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.5:93409356-93581320 on Build GRCh38 |
Assay Gene Location: | Within Exon 12 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NR2F1-AS1 | NR_021491.2 | 6 | 1109 | |
| NR_109820.1 | 5 | 1070 | ||
| NR_109821.1 | 7 | 1230 | ||
| NR_109822.1 | 3 | 1520 | ||
| NR_109823.1 | 5 | 1067 | ||
| NR_109824.1 | 6 | 1166 | ||
| NR_109825.1 | 9 | 2032 | ||
| AK124699.1 | 5 | 1795 | ||
| AK311143.1 | ||||
| BX647510.1 | 6 | 924 | ||
| DB168614.1 | 1 | 431 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv830402 | Chr.5:93368195 - 93511639 on Build GRCh38 | Gain |
 NR2F1-AS1
|
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Additional Information:
For this assay, SNP(s) [rs145798424] 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
Exonic
DGV Variation
|
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