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Variant : CV609149 (Single allele) Homo sapiens

Symbol: CV609149
Name: Single allele
Condition: Glioma [RCV000754871]
Clinical Significance: likely pathogenic
Last Evaluated: 06/05/2017
Review Status: no assertion criteria provided
Related Genes: ABHD17B   ACO1   ALDH1A1   ALDH1B1   ANKRD18A   ANKRD18B   ANKRD20A1   ANKRD20A2   ANKRD20A3   ANKRD20A4   ANXA1   APBA1   APTX   AQP3   AQP7   ARHGEF39   ARID3C   B4GALT1   BAG1   BANCR   C9orf131   C9orf135   C9orf24   C9orf40   C9orf57   C9orf64   C9orf72   C9orf85   CA9   CAAP1   CARNMT1   CARNMT1-AS1   CBWD3   CBWD5   CBWD6   CCDC107   CCIN   CCL19   CCL21   CCL27   CD72   CEMIP2   CEP78   CHMP5   CLTA   CNTFR   CNTNAP3   CNTNAP3B   CREB3   DCAF10   DCAF12   DCTN3   DDX58   DNAI1   DNAJA1   DNAJB5   ELAVL2   ENHO   EQTN   EXOSC3   FAM122A   FAM166B   FAM189A2   FAM205A   FAM214B   FAM219A   FAM221B   FAM27D1   FANCG   FBXO10   FOXB2   FOXD4L3   FOXD4L4   FOXD4L5   FOXD4L6   FRMD3   FRMPD1   FXN   GALT   GBA2   GCNT1   GDA   GKAP1   GLIPR2   GNA14   GNAQ   GNE   GRHPR   HINT2   HNRNPK   HRCT1   IDNK   IFT74   IGFBPL1   IL11RA   IZUMO3   KIF24   KIF27   KLF9   LINC00537   LINGO2   LRRC19   MAMDC2   MELK   MIR204   MIR7-1   MOB3B   MSMP   MYORG   NDUFB6   NFX1   NMRK1   NOL6   NPR2   NTRK2   NUDT2   OR13J1   OR2S2   OSTF1   PAX5   PCA3   PCSK5   PGM5   PHF24   PIGO   PIP5K1B   PLAA   POLR1E   PRKACG   PRSS3   PRUNE2   PSAT1   PTAR1   RASEF   RECK   RFK   RGP1   RMI1   RMRP   RNF38   RORB   RPP25L   RUSC2   SHB   SIGMAR1   SIT1   SLC25A51   SLC28A3   SMC5   SMU1   SPAG8   SPATA31A1   SPATA31A3   SPATA31A5   SPATA31A6   SPATA31A7   SPATA31D1   SPATA31D3   SPATA31D4   SPINK4   STOML2   TAF1L   TEK   TESK1   TJP2   TLE1   TLE4   TLN1   TMC1   TMEM215   TMEM252   TMEM8B   TOMM5   TOPORS   TPM2   TRMT10B   TRPM3   TRPM6   TUSC1   UBAP1   UBAP2   UBE2R2   UBQLN1   UNC13B   VCP   VPS13A   ZBTB5   ZCCHC7   ZFAND5   ZNF658  
Variant Type: complex (SO:0001784)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37923,524,426 - 87,359,888CLINVAR
Cytogenetic Map99p21.3-q21.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14393204
Created: 2019-03-12
Species: Homo sapiens
Last Modified: 2019-12-03
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.