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Variant : CV673665 (GRCh37/hg19 8q24.3(chr8:145645435-145881333)x1) Homo sapiens

Symbol: CV673665
Name: GRCh37/hg19 8q24.3(chr8:145645435-145881333)x1
Condition: not provided [RCV000846781]
Clinical Significance: uncertain significance
Last Evaluated: 06/26/2017
Review Status: no assertion criteria provided
Related Genes: ARHGAP39   C8orf82   CYHR1   FOXH1   GPT   KIFC2   LRRC14   LRRC24   MFSD3   PPP1R16A   RECQL4   TONSL   VPS28  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh378145,645,435 - 145,881,333CLINVAR
Cytogenetic Map88q24.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14977362
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-05-19
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.