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Variant : CV159723 (GRCh38/hg38 3q29(chr3:196812829-197938552)x3) Homo sapiens

Symbol: CV159723
Name: GRCh38/hg38 3q29(chr3:196812829-197938552)x3
Condition: See cases [RCV000138900]
Clinical Significance: uncertain significance
Last Evaluated: 08/14/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: BDH1   DLG1   DLG1-AS1   FYTTD1   IQCG   LINC02012   LRCH3   MELTF   MELTF-AS1   MIR4797   MIR922   NCBP2   NCBP2-AS1   NCBP2AS2   PAK2   PIGZ   RUBCN   SENP5  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_196812829)_(197938552_?)dup
NC_000003.11:g.(?_196539700)_(197665423_?)dup
NC_000003.10:g.(?_198024097)_(199149820_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh383196,812,829 - 197,938,552CLINVAR
GRCh373196,539,700 - 197,665,423CLINVAR
Build 363198,024,097 - 199,149,820CLINVAR
Cytogenetic Map33q29CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486433
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-08-04
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.