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Variant : CV158698 (GRCh38/hg38 3q26.32-29(chr3:176439911-198118383)x3) Homo sapiens

Symbol: CV158698
Name: GRCh38/hg38 3q26.32-29(chr3:176439911-198118383)x3
Condition: See cases [RCV000138009]
Clinical Significance: pathogenic|likely benign
Last Evaluated: 12/16/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ABCC5   ABCC5-AS1   ABCF3   AC007920.1   AC007920.2   AC072022.1   AC076966.2   AC107294.2   AC108734.4   ACAP2   ACTL6A   ADIPOQ   ADIPOQ-AS1   AHSG   ALG3   AP2M1   APOD   ATP11B   ATP13A3   ATP13A4   ATP13A4-AS1   ATP13A5   ATP13A5-AS1   B3GNT5   BCL6   BDH1   C3orf70   CAMK2N2   CCDC39   CCDC50   CEP19   CHRD   CLCN2   CLDN1   CLDN16   CPN2   CRYGS   DCUN1D1   DGKG   DLG1   DLG1-AS1   DNAJB11   DNAJC19   DVL3   ECE2   EEF1AKMT4   EEF1AKMT4-ECE2   EHHADH   EHHADH-AS1   EIF2B5   EIF4A2   EIF4G1   EPHB3   ETV5   FAM131A   FAM43A   FBXO45   FETUB   FGF12   FGF12-AS1   FGF12-AS2   FGF12-AS3   FLJ42393   FXR1   FYTTD1   GMNC   GNB4   GP5   HES1   HRG   HTR3C   HTR3D   HTR3E   HTR3E-AS1   IGF2BP2   IGF2BP2-AS1   IL1RAP   IQCG   KCNMB2   KCNMB2-AS1   KCNMB3   KLHL24   KLHL6   KLHL6-AS1   KNG1   LAMP3   LINC00501   LINC00578   LINC00884   LINC00885   LINC00887   LINC00888   LINC01014   LINC01063   LINC01206   LINC01208   LINC01209   LINC01839   LINC01840   LINC01968   LINC01972   LINC01983   LINC01991   LINC01994   LINC01995   LINC02012   LINC02013   LINC02015   LINC02020   LINC02026   LINC02028   LINC02031   LINC02036   LINC02037   LINC02038   LINC02041   LINC02043   LINC02048   LINC02052   LINC02053   LINC02054   LINC02069   LIPH   LMLN   LMLN-AS1   LPP   LPP-AS1   LPP-AS2   LRCH3   LRRC15   LSG1   MAGEF1   MAP3K13   MAP6D1   MASP1   MB21D2   MCCC1   MCF2L2   MELTF   MELTF-AS1   MFN1   MIR1224   MIR1248   MIR28   MIR3137   MIR4448   MIR4797   MIR548AQ   MIR5588   MIR570   MIR570HG   MIR6829   MIR7977   MIR922   MIR944   MRPL47   MUC20   MUC4   NCBP2   NCBP2-AS1   NCBP2AS2   NDUFB5   NRROS   OPA1   OPA1-AS1   OSTN   OSTN-AS1   P3H2   P3H2-AS1   PAK2   PARL   PCYT1A   PEX5L   PEX5L-AS2   PIGX   PIGZ   PIK3CA   PLAAT1   POLR2H   PPP1R2   PSMD2   PYDC2   RFC4   RNF168   RPL35A   RPL39L   RTP1   RTP2   RTP4   RUBCN   SENP2   SENP5   SLC51A   SMCO1   SNAR-I   SNORA4   SNORA63   SNORA63B   SNORA63D   SNORA63E   SNORA81   SNORD2   SNORD66   SOX2   SOX2-OT   SST   ST6GAL1   TBCCD1   TBL1XR1   TCTEX1D2   TFRC   THPO   TM4SF19   TM4SF19-AS1   TM4SF19-TCTEX1D2   TMEM207   TMEM41A   TMEM44   TMEM44-AS1   TNK2   TNK2-AS1   TP63   TPRG1   TPRG1-AS1   TPRG1-AS2   TRA2B   TTC14   UBXN7   UBXN7-AS1   USP13   UTS2B   VPS8   VWA5B2   WDR53   XXYLT1   XXYLT1-AS1   XXYLT1-AS2   YEATS2   YEATS2-AS1   ZDHHC19   ZMAT3   ZNF639  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_176439911)_(198118383_?)dup
Human AssemblyChrPosition (strand)Source
GRCh383176,439,911 - 198,118,383CLINVAR
GRCh373176,157,699 - 197,845,254CLINVAR
Build 363177,640,393 - 199,329,651CLINVAR
Cytogenetic Map33q26.32-29CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9485558
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-08-04
Status: ACTIVE


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