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Variant : CV163723 (GRCh38/hg38 3q29(chr3:195976744-197629463)x1) Homo sapiens

Symbol: CV163723
Name: GRCh38/hg38 3q29(chr3:195976744-197629463)x1
Condition: See cases [RCV000142155]
Clinical Significance: pathogenic
Last Evaluated: 10/29/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: BDH1   CEP19   DLG1   DLG1-AS1   FBXO45   LINC00885   LINC01063   LINC02012   MELTF   MELTF-AS1   MIR4797   NCBP2   NCBP2-AS1   NCBP2AS2   NRROS   PAK2   PCYT1A   PIGX   PIGZ   RNF168   SENP5   SLC51A   SMCO1   TCTEX1D2   TFRC   TM4SF19   TM4SF19-AS1   TM4SF19-TCTEX1D2   UBXN7   UBXN7-AS1   WDR53   ZDHHC19  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_195976744)_(197629463_?)del
Human AssemblyChrPosition (strand)Source
GRCh383195,976,744 - 197,629,463CLINVAR
GRCh373195,703,615 - 197,356,334CLINVAR
Build 363197,188,012 - 198,840,731CLINVAR
Cytogenetic Map33q29CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9489674
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-28
Status: ACTIVE


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