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Variant : CV383797 (GRCh37/hg19 10p15.3-14(chr10:2116123-8856296)x3) Homo sapiens

Symbol: CV383797
Name: GRCh37/hg19 10p15.3-14(chr10:2116123-8856296)x3
Condition: See cases [RCV000445989]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: AKR1C1   AKR1C2   AKR1C3   AKR1C4   AKR1E2   ANKRD16   ASB13   ATP5F1C   CALML3   CALML3-AS1   CALML5   FBH1   GATA3   GDI2   IL15RA   IL2RA   ITIH2   ITIH5   KIN   KLF6   NET1   PFKFB3   PFKP   PITRM1   PRKCQ   RBM17   SFMBT2   TAF3   TASOR2   TUBAL3   UCN3  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37102,116,123 - 8,856,296CLINVAR
Cytogenetic Map1010p15.3-14CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 12850718
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-11-17
Status: ACTIVE


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