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Variant : CV673646 (GRCh37/hg19 3q29(chr3:195701149-197348561)x3) Homo sapiens

Symbol: CV673646
Name: GRCh37/hg19 3q29(chr3:195701149-197348561)x3
Condition: not provided [RCV000846762]
Clinical Significance: pathogenic
Last Evaluated: 08/18/2017
Review Status: no assertion criteria provided
Related Genes: BDH1   CEP19   DLG1   FBXO45   MELTF   NCBP2   NRROS   PAK2   PCYT1A   PIGX   PIGZ   RNF168   SENP5   SLC51A   SMCO1   TCTEX1D2   TFRC   TM4SF19   UBXN7   WDR53   ZDHHC19  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh373195,701,149 - 197,348,561CLINVAR
Cytogenetic Map33q29CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14977344
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-03-17
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.