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Variant : CV73371 (GRCh38/hg38 10q23.33-24.2(chr10:92626680-97755102)x1) Homo sapiens

Symbol: CV73371
Name: GRCh38/hg38 10q23.33-24.2(chr10:92626680-97755102)x1
Condition: Hydronephrosis [RCV000052564]|See cases [RCV000052564]
Clinical Significance: pathogenic
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: ACSM6   ALDH18A1   ANKRD2   ARHGAP19   ARHGAP19-SLIT1   AVPI1   BLNK   C10orf62   CC2D2B   CCNJ   CEP55   CYP26A1   CYP26C1   CYP2C18   CYP2C19   CYP2C8   CYP2C9   DNTT   ENTPD1   ENTPD1-AS1   EXOC6   EXOSC1   FFAR4   FRA10AC1   FRAT1   FRAT2   HELLS   HHEX   HOGA1   KIF11   LCOR   LGI1   MARVELD1   MIR3157   MIR607   MMS19   MORN4   MYOF   NOC3L   OPALIN   PDE6C   PDLIM1   PGAM1   PI4K2A   PIK3AP1   PLCE1   PLCE1-AS1   PLCE1-AS2   RBP4   RRP12   SLC35G1   SLIT1   SLIT1-AS1   SORBS1   TBC1D12   TCTN3   TLL2   TM9SF3   UBTD1   ZDHHC16   ZFYVE27   ZNF518A  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_92626680)_(97755102_?)del
NC_000010.10:g.(?_94386437)_(99514859_?)del
NC_000010.9:g.(?_94376417)_(99504849_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381092,626,680 - 97,755,102CLINVAR
GRCh371094,386,437 - 99,514,859CLINVAR
Build 361094,376,417 - 99,504,849CLINVAR
Cytogenetic Map1010q23.33-24.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8619540
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2020-02-11
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.