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Variant : CV157767 (GRCh38/hg38 3q29(chr3:195711798-198110178)x3) Homo sapiens

Symbol: CV157767
Name: GRCh38/hg38 3q29(chr3:195711798-198110178)x3
Condition: See cases [RCV000137110]
Clinical Significance: pathogenic
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: BDH1   CEP19   DLG1   DLG1-AS1   FBXO45   FYTTD1   IQCG   LINC00885   LINC01063   LINC01983   LINC02012   LMLN   LMLN-AS1   LRCH3   MELTF   MELTF-AS1   MIR4797   MIR570HG   MIR6829   MIR922   MUC20   MUC4   NCBP2   NCBP2-AS1   NCBP2AS2   NRROS   PAK2   PCYT1A   PIGX   PIGZ   RNF168   RPL35A   RUBCN   SENP5   SLC51A   SMCO1   TCTEX1D2   TFRC   TM4SF19   TM4SF19-AS1   TM4SF19-TCTEX1D2   TNK2   TNK2-AS1   UBXN7   UBXN7-AS1   WDR53   ZDHHC19  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_195711798)_(198110178_?)dup
Human AssemblyChrPosition (strand)Source
GRCh383195,711,798 - 198,110,178CLINVAR
GRCh373195,438,669 - 197,837,049CLINVAR
Build 363196,924,340 - 199,321,446CLINVAR
Cytogenetic Map33q29CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9484669
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.