Assay Details
Target Gene Details
Entrez Gene ID: | 650669 |
Gene Name: | GAS6 antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.13:113815610-113842841 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
GAS6-AS1 | NR_044995.2 | |||
BX385300.2 | ||||
DA460725.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv563390 | Chr.13:113809317 - 113845944 on Build GRCh38 | Loss | GAS6-AS1 TMEM255B GAS6 |
nsv563396 | Chr.13:113802932 - 113820249 on Build GRCh38 | Loss | GAS6-AS1 TMEM255B |
nsv1043348 | Chr.13:113756321 - 113867896 on Build GRCh38 | Gain | GAS6-AS1 GAS6-AS2 LOC105377805 TMEM255B GAS6 |
dgv3451n54 | Chr.13:113810996 - 113820661 on Build GRCh38 | Loss | GAS6-AS1 TMEM255B GAS6 |
nsv951933 | Chr.13:113808028 - 113844427 on Build GRCh38 | Deletion | GAS6-AS1 TMEM255B GAS6 |
dgv3450n54 | Chr.13:113754200 - 113886735 on Build GRCh38 | Gain | GAS6-AS1 GAS6-AS2 LOC105377805 TMEM255B GAS6 LINC00454 |
nsv832727 | Chr.13:113753115 - 113918257 on Build GRCh38 | Loss | GAS6-AS1 GAS6-AS2 LOC105377805 TMEM255B LINC00452 GAS6 LINC00454 |
esv3633615 | Chr.13:113724844 - 113843481 on Build GRCh38 | Gain | GAS6-AS1 LOC105377805 TMEM255B GAS6 LINC00552 GRK1 |
esv24756 | Chr.13:113802553 - 113834906 on Build GRCh38 | Gain+Loss | GAS6-AS1 TMEM255B GAS6 |
esv3582860 | Chr.13:113756381 - 113867871 on Build GRCh38 | Gain | GAS6-AS1 GAS6-AS2 LOC105377805 TMEM255B GAS6 |
nsv826836 | Chr.13:113753163 - 113875076 on Build GRCh38 | Loss | GAS6-AS1 GAS6-AS2 LOC105377805 TMEM255B GAS6 |
nsv563392 | Chr.13:113814175 - 113823135 on Build GRCh38 | Loss | GAS6-AS1 GAS6 |
nsv826837 | Chr.13:113802020 - 113834906 on Build GRCh38 | Loss | GAS6-AS1 TMEM255B GAS6 |
esv3633622 | Chr.13:113808937 - 113835264 on Build GRCh38 | Gain | GAS6-AS1 TMEM255B GAS6 |
More Information
Additional Information:
For this assay, SNP(s) [rs72670688] 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 |