Assay Details
Target Gene Details
Entrez Gene ID: | 23786 |
Gene Name: | BCL2 like 13 |
Gene Aliases: |
BCL-RAMBO, Bcl2-L-13, MIL1 |
Location: |
Chr.22:17628855-17730855 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv588106 | Chr.22:17659162 - 17662058 on Build GRCh38 | Gain | BCL2L13 |
esv2673622 | Chr.22:17657329 - 17662076 on Build GRCh38 | Deletion | BCL2L13 |
nsv588107 | Chr.22:17659737 - 17661069 on Build GRCh38 | Loss | BCL2L13 |
esv3893429 | Chr.22:17600825 - 17678777 on Build GRCh38 | Gain | BCL2L13 ATP6V1E1 |
esv3893428 | Chr.22:17578563 - 18040448 on Build GRCh38 | Loss | MICAL3 BCL2L13 MIR3198-1 SLC25A18 FLJ41941 ATP6V1E1 MIR648 LINC00528 LOC101929372 BID |
nsv428385 | Chr.22:17491941 - 18886703 on Build GRCh38 | Gain+Loss | MICAL3 MIR3198-1 FLJ41941 ATP6V1E1 MIR648 LOC642643 PI4KAP1 PEX26 LOC729461 TMEM191B LOC100996432 USP18 LOC101929372 GGT3P RIMBP3 LOC100996415 LINC00528 FAM230A LOC100996401 CECR2 BCL2L13 LOC102725072 SLC25A18 TUBA8 BID |
esv1008890 | Chr.22:17657148 - 17667590 on Build GRCh38 | Deletion | BCL2L13 |
esv3647231 | Chr.22:17658930 - 17661862 on Build GRCh38 | Loss | BCL2L13 |
nsv828929 | Chr.22:17658015 - 17662018 on Build GRCh38 | Gain | BCL2L13 |
nsv9871 | Chr.22:17545048 - 17683541 on Build GRCh38 | Loss | BCL2L13 SLC25A18 ATP6V1E1 LOC101929372 CECR2 |
nsv526826 | Chr.22:17411511 - 17836413 on Build GRCh38 | Gain | MICAL3 BCL2L13 MIR3198-1 SLC25A18 ATP6V1E1 LINC00528 LOC101929372 BID CECR2 |
dgv4465n100 | Chr.22:17577691 - 17706530 on Build GRCh38 | Gain | BCL2L13 SLC25A18 ATP6V1E1 LOC101929372 |
nsv1146118 | Chr.22:17658929 - 17661865 on Build GRCh38 | Deletion | BCL2L13 |
esv3557908 | Chr.22:17658735 - 17662050 on Build GRCh38 | Deletion | BCL2L13 |
esv28002 | Chr.22:17658736 - 17661690 on Build GRCh38 | Loss | BCL2L13 |
More Information
Additional Information:
For this assay, SNP(s) [rs143728189] 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 |