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Variant : CV436251 (GRCh37/hg19 10p15.3-13(chr10:100026-12842179)x1) Homo sapiens

Symbol: CV436251
Name: GRCh37/hg19 10p15.3-13(chr10:100026-12842179)x1
Condition: See cases [RCV000512541]
Clinical Significance: pathogenic
Last Evaluated: 12/02/2014
Review Status: no assertion criteria provided
Related Genes: ADARB2   AKR1C1   AKR1C2   AKR1C3   AKR1C4   AKR1E2   ANKRD16   ASB13   ATP5F1C   CALML3   CALML3-AS1   CALML5   CAMK1D   CDC123   CELF2   DHTKD1   DIP2C   ECHDC3   FBH1   GATA3   GDI2   GTPBP4   IDI1   IDI2   IL15RA   IL2RA   ITIH2   ITIH5   KIN   KLF6   LARP4B   NET1   NUDT5   PFKFB3   PFKP   PITRM1   PRKCQ   PROSER2   RBM17   SEC61A2   SFMBT2   TAF3   TASOR2   TUBAL3   UCN3   UPF2   USP6NL   WDR37   ZMYND11  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710100,026 - 12,842,179CLINVAR
Cytogenetic Map1010p15.3-13CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13445503
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-11-17
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.