Assay Details
Target Gene Details
Entrez Gene ID: | 100130950 |
Gene Name: | uncharacterized LOC100130950 |
Gene Aliases: |
- |
Location: |
Chr.17:5192084-5235636 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC100130950 | NR_034082.1 | |||
AK021878.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv574273 | Chr.17:4585589 - 5460332 on Build GRCh38 | Gain | MIR6864 PFN1 ZFP3 SLC52A1 CXCL16 PELP1 MINK1 ZNF232 PLD2 USP6 LOC101928000 ZMYND15 GLTPD2 C1QBP ZNF594 KIF1C ALOX15 PSMB6 ARRB2 SPAG7 LOC101559451 LOC102724009 LOC400568 SLC25A11 NUP88 C17orf107 TM4SF5 INCA1 DHX33 GP1BA CHRNE ENO3 SCIMP VMO1 LOC101927979 LOC100130950 RPAIN SMTNL2 RABEP1 LOC107984973 MIR6865 CAMTA2 RNF167 MED11 |
dgv3089n100 | Chr.17:5187013 - 5327634 on Build GRCh38 | Gain | SCIMP LOC100130950 RABEP1 ZNF594 |
More Information
Additional Information:
For this assay, SNP(s) [rs73333445] 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 |