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Variant : CV513795 (GRCh37/hg19 2q12.1-24.3(chr2:104172062-168223828)x1) Homo sapiens

Symbol: CV513795
Name: GRCh37/hg19 2q12.1-24.3(chr2:104172062-168223828)x1
Condition: PARP Inhibitor response [RCV000626436]
Clinical Significance: drug response
Last Evaluated: 11/27/2017
Review Status: no assertion criteria provided
Related Genes: ACMSD   ACOXL   ACTR3   ACVR1   ACVR1C   ACVR2A   AMER3   AMMECR1L   ANAPC1   ARHGAP15   ARHGEF4   ARL5A   ARL6IP6   BAZ2B   BCL2L11   BIN1   BUB1   C1QL2   C2orf27A   C2orf27B   C2orf49   C2orf76   CACNB4   CBWD2   CCDC115   CCDC138   CCDC148   CCDC74A   CCDC74B   CCDC93   CCNT2   CD302   CFC1   CFC1B   CHCHD5   CKAP2L   CLASP1   CNTNAP5   COBLL1   CSRNP3   CXCR4   CYP27C1   CYTIP   DAPL1   DARS1   DBI   DDX18   DPP10   DPP4   ECRG4   EDAR   EN1   EPB41L5   EPC2   ERCC3   ERMN   FAM168B   FAP   FBLN7   FHL2   FIGN   FMNL2   FOXD4L1   GALNT13   GALNT3   GALNT5   GCA   GCC2   GCG   GLI2   GPD2   GPR148   GPR17   GPR39   GPR45   GRB14   GTDC1   GYPC   HNMT   HS6ST1   IFIH1   IL1A   IL1B   IL1F10   IL1RN   IL36A   IL36B   IL36G   IL36RN   IL37   IMP4   INHBB   INSIG2   ITGB6   IWS1   KCNH7   KCNJ3   KYNU   LCT   LIMS1   LIMS2   LIMS3   LIMS4   LRP1B   LY75   LY75-CD302   LYPD1   LYPD6   LYPD6B   MALL   MAP3K19   MAP3K2   MARCHF7   MARCO   MBD5   MCM6   MERTK   MGAT5   MIR128-1   MMADHC   MRPS9   MYO7B   MZT2A   MZT2B   NCK2   NCKAP5   NEB   NIFK   NMI   NPHP1   NR4A2   NT5DC4   NXPH2   ORC4   PAX8   PKP4   PLA2R1   PLEKHB2   POLR1B   POLR2D   POTEE   POTEF   POTEI   POTEJ   POU3F3   PROC   PRPF40A   PSD4   PSMD14   PTPN18   PTPN4   R3HDM1   RAB3GAP1   RAB6C   RABL2A   RALB   RANBP2   RBM43   RBMS1   RGPD3   RGPD4   RGPD5   RGPD6   RGPD8   RIF1   RND3   RNU4ATAC   RPRM   SAP130   SCN1A   SCN2A   SCN3A   SCN7A   SCN9A   SCTR   SEPTIN10   SFT2D3   SLC20A1   SLC35F5   SLC38A11   SLC4A10   SLC5A7   SMPD4   SOWAHC   SPOPL   ST6GAL2   STAM2   STEAP3   SULT1C2   SULT1C3   SULT1C4   TANC1   TANK   TBR1   TFCP2L1   TGFBRAP1   THSD7B   TMEM163   TMEM177   TMEM185B   TMEM37   TMEM87B   TNFAIP6   TSN   TTC21B   TTL   TUBA3D   TUBA3E   UBXN4   UGGT1   UPP2   UXS1   WDR33   WDSUB1   XIRP2   ZC3H6   ZC3H8   ZEB2   ZNF806   ZRANB3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372104,172,062 - 168,223,828CLINVAR
Cytogenetic Map22q12.1-24.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13613359
Created: 2018-06-12
Species: Homo sapiens
Last Modified: 2020-03-24
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.