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Variant : CV382959 (GRCh37/hg19 8q13.2-13.3(chr8:69899336-72597645)x1) Homo sapiens

Symbol: CV382959
Name: GRCh37/hg19 8q13.2-13.3(chr8:69899336-72597645)x1
Condition: See cases [RCV000446721]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: EYA1   LACTB2   NCOA2   PRDM14   SLCO5A1   SULF1   TRAM1   XKR9  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37869,899,336 - 72,597,645CLINVAR
Cytogenetic Map88q13.2-13.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12851444
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-03-31
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.