Assay Details
Target Gene Details
Entrez Gene ID: | 9717 |
Gene Name: | SEC14 like lipid binding 5 |
Gene Aliases: |
PRELID4B |
Location: |
Chr.16:4958317-5019155 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SEC14L5 | NM_014692.1 | NP_055507.1 | ||
AB007880.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3637714 | Chr.16:4958035 - 5079276 on Build GRCh38 | Gain | NAGPA NAGPA-AS1 SEC14L5 ALG1 C16orf89 |
esv3637713 | Chr.16:4957958 - 5307305 on Build GRCh38 | Gain | EEF2KMT RBFOX1 NAGPA NAGPA-AS1 SEC14L5 ALG1 C16orf89 |
esv25186 | Chr.16:4858500 - 5142800 on Build GRCh38 | Gain | EEF2KMT UBN1 NAGPA NAGPA-AS1 PPL SEC14L5 ALG1 C16orf89 |
esv2761893 | Chr.16:4941276 - 4995458 on Build GRCh38 | Loss | SEC14L5 |
esv3892763 | Chr.16:4971982 - 4977763 on Build GRCh38 | Loss | SEC14L5 |
esv2422516 | Chr.16:4775920 - 5160979 on Build GRCh38 | Deletion | GLYR1 EEF2KMT UBN1 NAGPA NAGPA-AS1 ROGDI PPL SEC14L5 ALG1 C16orf89 SEPT12 SMIM22 |
nsv1046986 | Chr.16:4049000 - 5555721 on Build GRCh38 | Gain | HMOX2 PAM16 PPL NUDT16L1 LINC01569 MGRN1 CORO7-PAM16 GLYR1 MIR6769A EEF2KMT DNAJA3 GLIS2-AS1 ROGDI SRL SEPT12 LOC105371063 UBN1 NAGPA ZNF500 SMIM22 C16orf71 UBALD1 CDIP1 ANKS3 VASN NMRAL1 RBFOX1 NAGPA-AS1 GLIS2 C16orf96 SEC14L5 CORO7 ADCY9 ALG1 C16orf89 TFAP4 |
nsv1042612 | Chr.16:4965694 - 5150514 on Build GRCh38 | Loss | EEF2KMT NAGPA NAGPA-AS1 SEC14L5 ALG1 C16orf89 |
nsv457360 | Chr.16:4960912 - 5284683 on Build GRCh38 | Loss | EEF2KMT RBFOX1 NAGPA NAGPA-AS1 SEC14L5 ALG1 C16orf89 |
nsv528586 | Chr.16:4951303 - 5021669 on Build GRCh38 | Gain | SEC14L5 |
esv2760069 | Chr.16:4922849 - 5374828 on Build GRCh38 | Gain+Loss | EEF2KMT RBFOX1 NAGPA NAGPA-AS1 PPL SEC14L5 ALG1 C16orf89 |
esv3892762 | Chr.16:4967386 - 5060625 on Build GRCh38 | Gain | NAGPA NAGPA-AS1 SEC14L5 C16orf89 |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |