Assay Details
Target Gene Details
Entrez Gene ID: | 2323 |
Gene Name: | fms related tyrosine kinase 3 ligand |
Gene Aliases: |
FL, FLT3L |
Location: |
Chr.19:49474172-49487038 on Build GRCh38 |
Assay Gene Location: | Within Intron 9 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv9739 | Chr.19:47901840 - 50143063 on Build GRCh38 | Gain+Loss | MIR4750 SNAR-C5 PNKP LOC105372430 AP2A1 MIR4324 SNORD35B PRR12 BCAT2 IL4I1 SNAR-B1 MIR150 BAX LOC101928295 NTN5 CGB8 SPHK2 TEAD2 AKT1S1 SNAR-A12 FAM83E SLC6A16 LOC105447645 MED25 PPFIA3 NUCB1-AS1 FCGRT CCDC155 MIR6799 RRAS PLEKHA4 FLJ26850 LMTK3 CD37 GFY SNAR-A6 FUT1 C19orf73 RPS11 GRWD1 ATF5 SULT2B1 VRK3 SNORD32A LHB SEC1P SIGLEC16 MIR6800 SNAR-A7 SNAR-A13 SPACA4 FGF21 CGB7 CGB5 CGB1 SIGLEC11 LIG1 CCDC114 PLA2G4C TULP2 BCL2L12 CPT1C RUVBL2 IRF3 RASIP1 C19orf68 CABP5 CA11 SNAR-A2 ALDH16A1 KDELR1 PRMT1 ELSPBP1 SNAR-A3 CGB2 SNORD35A NUP62 SNAR-G2 DKKL1 RPL13A CARD8 MIR6798 TBC1D17 PPP1R15A CARD8-AS1 MIR4751 SNAR-G1 HSD17B14 SCAF1 FTL KCNA7 BSPH1 TRPM4 SNAR-A8 PTH2 MIR5088 PTOV1-AS1 SNAR-A5 SLC17A7 IZUMO1 EMP3 SNAR-A14 KCNJ14 PIH1D1 PLA2G4C-AS1 NTF4 NUCB1 PTOV1 DBP RPL18 SNAR-B2 ADM5 LOC100287477 SNAR-A10 SNORD33 SNAR-C1 FLT3LG HRC LOC101059948 SNAR-C2 DHDH CYTH2 FUT2 SNORD34 SNAR-A11 MAMSTR MIR4749 GRIN2D ZNF473 SYNGR4 SNAR-D GYS1 TMEM143 CGB3 PRRG2 SNAR-C4 NOSIP LIN7B RCN3 SNAR-C3 SNRNP70 SNAR-A9 TSKS SNAR-A4 FUZ ZNF114 SNAR-A1 PTOV1-AS2 |
nsv833863 | Chr.19:49479177 - 49629716 on Build GRCh38 | Loss | RPS11 SNORD33 SNORD32A FLT3LG FCGRT RPL13A PRRG2 SNORD35B NOSIP PRR12 SNORD34 MIR150 RCN3 SNORD35A |
nsv833862 | Chr.19:49448789 - 49570676 on Build GRCh38 | Loss | RPS11 SNORD33 SNORD32A FLT3LG FCGRT RPL13A SNORD35B NOSIP SNORD34 MIR150 RCN3 PIH1D1 ALDH16A1 SNORD35A |
nsv953599 | Chr.19:49386444 - 49506743 on Build GRCh38 | Deletion | RPS11 SNORD33 SNORD32A FLT3LG RPL13A PTH2 CCDC155 SNORD35B SLC17A7 SNORD34 MIR150 PIH1D1 LOC101928295 ALDH16A1 SNORD35A GFY |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |