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Variant : CV381376 (GRCh37/hg19 19p13.2(chr19:10286133-11040457)x1) Homo sapiens

Symbol: CV381376
Name: GRCh37/hg19 19p13.2(chr19:10286133-11040457)x1
Condition: See cases [RCV000446752]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: AP1M2   ATG4D   C19orf38   CARM1   CDC37   CDKN2D   DNM2   DNMT1   FDX2   ICAM1   ICAM3   ICAM4   ICAM5   ILF3   KEAP1   KRI1   MIR199A1   MRPL4   PDE4A   QTRT1   RAVER1   S1PR2   S1PR5   SLC44A2   TIMM29   TMED1   TYK2   YIPF2   ZGLP1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371910,286,133 - 11,040,457CLINVAR
Cytogenetic Map1919p13.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12851475
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2019-11-12
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.