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Variant : CV158512 (GRCh38/hg38 3q29(chr3:192752937-198118383)x3) Homo sapiens

Symbol: CV158512
Name: GRCh38/hg38 3q29(chr3:192752937-198118383)x3
Condition: See cases [RCV000137827]
Clinical Significance: pathogenic
Last Evaluated: 10/07/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ACAP2   APOD   ATP13A3   ATP13A4   ATP13A4-AS1   ATP13A5   ATP13A5-AS1   BDH1   CEP19   CPN2   DLG1   DLG1-AS1   FAM43A   FBXO45   FYTTD1   GP5   HES1   IQCG   LINC00884   LINC00885   LINC00887   LINC01063   LINC01968   LINC01972   LINC01983   LINC02012   LINC02026   LINC02028   LINC02036   LINC02037   LINC02038   LINC02048   LMLN   LMLN-AS1   LRCH3   LRRC15   LSG1   MB21D2   MELTF   MELTF-AS1   MIR3137   MIR4797   MIR570   MIR570HG   MIR6829   MIR922   MUC20   MUC4   NCBP2   NCBP2-AS1   NCBP2AS2   NRROS   OPA1   OPA1-AS1   PAK2   PCYT1A   PIGX   PIGZ   PLAAT1   PPP1R2   RNF168   RPL35A   RUBCN   SENP5   SLC51A   SMCO1   TCTEX1D2   TFRC   TM4SF19   TM4SF19-AS1   TM4SF19-TCTEX1D2   TMEM44   TMEM44-AS1   TNK2   TNK2-AS1   UBXN7   UBXN7-AS1   WDR53   XXYLT1   XXYLT1-AS1   XXYLT1-AS2   ZDHHC19  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_192752937)_(198118383_?)dup
Human AssemblyChrPosition (strand)Source
GRCh383192,752,937 - 198,118,383CLINVAR
GRCh373192,470,726 - 197,845,254CLINVAR
Build 363193,953,420 - 199,329,651CLINVAR
Cytogenetic Map33q29CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9485379
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.