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Variant : CV513791 (GRCh37/hg19 6q21-23.2(chr6:112939290-132327952)x1) Homo sapiens

Symbol: CV513791
Name: GRCh37/hg19 6q21-23.2(chr6:112939290-132327952)x1
Condition: PARP Inhibitor response [RCV000626432]
Clinical Significance: drug response
Last Evaluated: 11/27/2017
Review Status: no assertion criteria provided
Related Genes: AKAP7   ARG1   ARHGAP18   ASF1A   C6orf58   CALHM4   CALHM5   CALHM6   CCN2   CENPW   CEP85L   CLVS2   COL10A1   CTAGE9   DCBLD1   DSE   ECHDC1   ENPP1   ENPP3   EPB41L2   FABP7   FAM162B   FAM184A   FRK   GJA1   GOPC   GPRC6A   HDAC2   HDDC2   HEY2   HINT3   HS3ST5   HSF2   KIAA0408   KPNA5   L3MBTL3   LAMA2   MAN1A1   MARCKS   MCM9   MED23   NCOA7   NKAIN2   NT5DC1   NUS1   OR2A4   PKIB   PLN   PTPRK   RFX6   RNF146   RNF217   RNF217-AS1   ROS1   RSPH4A   RSPO3   RWDD1   SAMD3   SERINC1   SLC35F1   SMLR1   SMPDL3A   SOGA3   TBC1D32   THEMIS   TMEM200A   TMEM244   TPD52L1   TRAPPC3L   TRDN   TRMT11   TSPYL1   TSPYL4   VGLL2   ZUP1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh376112,939,290 - 132,327,952CLINVAR
Cytogenetic Map66q21-23.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13613326
Created: 2018-06-12
Species: Homo sapiens
Last Modified: 2020-01-14
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.