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Variant : CV154699 (GRCh38/hg38 8q24.3(chr8:144264907-144668170)x1) Homo sapiens

Symbol: CV154699
Name: GRCh38/hg38 8q24.3(chr8:144264907-144668170)x1
Condition: See cases [RCV000134352]
Clinical Significance: benign
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADCK5   ARHGAP39   BOP1   C8orf82   CPSF1   CYHR1   DGAT1   FBXL6   FOXH1   GPT   HSF1   KIFC2   LRRC14   LRRC24   MFSD3   MIR10400   MIR1234   MIR6848   MIR6849   MIR6893   MIR939   PPP1R16A   RECQL4   SCRT1   SCX   SLC39A4   SLC52A2   TMEM249   TONSL   TONSL-AS1   VPS28  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_144264907)_(144668170_?)del
Human AssemblyChrPosition (strand)Source
GRCh388144,264,907 - 144,668,170CLINVAR
GRCh378145,319,810 - 145,893,555CLINVAR
Build 368145,391,798 - 145,864,363CLINVAR
Cytogenetic Map88q24.3CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 9481932
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
Status: ACTIVE


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