Assay Details
Target Gene Details
Entrez Gene ID: | 5273 |
Gene Name: | serpin family B member 10 |
Gene Aliases: |
PI-10, PI10 |
Location: |
Chr.18:63907969-63936111 on Build GRCh38 |
Assay Gene Location: | Within Intron 7 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SERPINB10 | NM_005024.2 | NP_005015.1 | ||
XM_011526027.1 | XP_011524329.1 | |||
XM_011526028.1 | XP_011524330.1 | |||
XM_017025793.1 | XP_016881282.1 | |||
XM_017025794.1 | XP_016881283.1 | |||
AK314936.1 | ||||
BC096217.3 | AAH96217.1 | |||
BC096218.3 | AAH96218.1 | |||
BC096219.3 | AAH96219.1 | |||
BC096220.3 | AAH96220.1 | |||
U35459.1 | AAC50282.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1066552 | Chr.18:63147299 - 64608176 on Build GRCh38 | Gain | SERPINB12 KDSR LINC00305 SERPINB5 LOC284294 SERPINB4 HMSD SERPINB3 SERPINB13 VPS4B SERPINB10 SERPINB7 SERPINB8 LINC01538 BCL2 SERPINB2 SERPINB11 |
nsv833673 | Chr.18:63897072 - 64097021 on Build GRCh38 | Gain | SERPINB10 SERPINB8 LINC00305 SERPINB2 HMSD |
esv3642785 | Chr.18:63831255 - 63986077 on Build GRCh38 | Gain | SERPINB10 SERPINB8 SERPINB2 HMSD |
esv21739 | Chr.18:63715122 - 64278129 on Build GRCh38 | Gain | SERPINB10 SERPINB7 SERPINB8 LINC01538 LINC00305 LOC284294 SERPINB2 SERPINB11 HMSD |
nsv1067311 | Chr.18:63818011 - 66637685 on Build GRCh38 | Loss | SERPINB10 CDH7 SERPINB8 LINC01538 LINC00305 CDH19 LOC284294 SERPINB2 HMSD |
nsv525889 | Chr.18:63845132 - 63948110 on Build GRCh38 | Loss | SERPINB10 SERPINB2 |
esv3642788 | Chr.18:63922332 - 63954216 on Build GRCh38 | Gain | SERPINB10 HMSD |
More Information
Additional Information:
For this assay, SNP(s) [rs73961817] 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 |