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Variant : CV364269 (GRCh37/hg19 10q23.1-25.1(chr10:85557432-105804295)x1) Homo sapiens

Symbol: CV364269
Name: GRCh37/hg19 10q23.1-25.1(chr10:85557432-105804295)x1
Condition: Metastatic prostate carcinoma [RCV000431909]|PARP Inhibitor response [RCV000431909]
Clinical Significance: pathogenic|drug response
Last Evaluated: 11/27/2017
Review Status: no assertion criteria provided
Related Genes: ABCC2   ACSM6   ACTA2   ACTR1A   ADIRF   ADIRF-AS1   AGAP11   ALDH18A1   ANKRD1   ANKRD2   ANKRD22   ARHGAP19   ARL3   ARMH3   AS3MT   ATAD1   ATP5MD   AVPI1   BLNK   BLOC1S2   BMPR1A   BORCS7   BTAF1   BTRC   C10orf62   C10orf95   C10orf99   CALHM1   CALHM2   CALHM3   CC2D2B   CCNJ   CCSER2   CDHR1   CEP55   CH25H   CHUK   CNNM1   CNNM2   COL17A1   COX15   CPEB3   CPN1   CRTAC1   CUEDC2   CUTC   CWF19L1   CYP17A1   CYP26A1   CYP26C1   CYP2C18   CYP2C19   CYP2C8   CYP2C9   DNMBP   DNTT   DPCD   ELOVL3   ENTPD1   ENTPD7   ERLIN1   EXOC6   EXOSC1   FAM25A   FAS   FAS-AS1   FBXL15   FBXW4   FFAR4   FGF8   FGFBP3   FRA10AC1   FRAT1   FRAT2   GBF1   GHITM   GLUD1   GOLGA7B   GOT1   GRID1   HECTD2   HELLS   HHEX   HIF1AN   HOGA1   HPS1   HPS6   HPSE2   HTR7   IDE   IFIT1   IFIT1B   IFIT2   IFIT3   IFIT5   INA   KAZALD1   KCNIP2   KIF11   KIF20B   KLLN   LBX1   LCOR   LDB1   LDB3   LGI1   LINC01520   LIPA   LIPF   LIPJ   LIPK   LIPM   LIPN   LOXL4   LRIT1   LRIT2   LZTS2   MARCHF5   MARVELD1   MFSD13A   MINPP1   MIR107   MIR146B   MIR346   MMRN2   MMS19   MORN4   MRPL43   MYOF   NDUFB8   NEURL1   NFKB2   NKX2-3   NOC3L   NOLC1   NPM3   NT5C2   NUTM2A   OGA   OPALIN   OPN4   PANK1   PAPSS2   PAX2   PCGF5   PCGF6   PDCD11   PDE6C   PDLIM1   PDZD7   PGAM1   PI4K2A   PIK3AP1   PITX3   PKD2L1   PLCE1   POLL   PPP1R3C   PPRC1   PSD   PTEN   PYROXD2   R3HCC1L   RBP4   RGR   RNLS   RPP30   RRP12   SCD   SEC31B   SEMA4G   SFRP5   SFXN2   SFXN3   SH3PXD2A   SHLD2   SLC16A12   SLC25A28   SLC35G1   SLF2   SLIT1   SLK   SNCG   SNORA12   SORBS1   STAMBPL1   STN1   SUFU   TAF5   TBC1D12   TCTN3   TLL2   TLX1   TLX1NB   TM9SF3   TNKS2   TRIM8   TWNK   UBTD1   WAPL   WBP1L   WNT8B   ZDHHC16   ZFYVE27   ZNF518A  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371085,557,432 - 105,804,295CLINVAR
Cytogenetic Map1010q23.1-25.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12841062
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-01-21
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.