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Variant : CV435796 (GRCh37/hg19 3q29(chr3:195456034-197356334)x3) Homo sapiens

Symbol: CV435796
Name: GRCh37/hg19 3q29(chr3:195456034-197356334)x3
Condition: See cases [RCV000512582]
Clinical Significance: uncertain significance
Last Evaluated: 10/22/2014
Review Status: no assertion criteria provided
Related Genes: BDH1   CEP19   DLG1   FBXO45   MELTF   MUC20   MUC4   NCBP2   NRROS   PAK2   PCYT1A   PIGX   PIGZ   RNF168   SENP5   SLC51A   SMCO1   TCTEX1D2   TFRC   TM4SF19   TNK2   TNK2-AS1   UBXN7   WDR53   ZDHHC19  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh373195,456,034 - 197,356,334CLINVAR
Cytogenetic Map33q29CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13445543
Created: 2017-11-07
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.