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Variant : CV592779 (GRCh37/hg19 12q24.31(chr12:122706844-124294517)x3) Homo sapiens

Symbol: CV592779
Name: GRCh37/hg19 12q24.31(chr12:122706844-124294517)x3
Condition: not provided [RCV000738079]
Clinical Significance: uncertain significance
Last Evaluated: 11/16/2010
Review Status: no assertion criteria provided
Related Genes: ABCB9   ARL6IP4   ATP6V0A2   C12orf65   CCDC62   CDK2AP1   CLIP1   DDX55   DENR   DIABLO   DNAH10   EIF2B1   GTF2H3   HCAR1   HCAR2   HCAR3   HIP1R   KMT5A   KNTC1   MPHOSPH9   OGFOD2   PITPNM2   RILPL1   RILPL2   RSRC2   SBNO1   SNRNP35   TCTN2   TMED2   VPS33A   VPS37B   ZCCHC8  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3712122,706,844 - 124,294,517CLINVAR
Cytogenetic Map1212q24.31CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14350544
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-03-24
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.