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Variant : CV437589 (GRCh37/hg19 9p24.3(chr9:203861-539781)x1) Homo sapiens

Symbol: CV437589
Name: GRCh37/hg19 9p24.3(chr9:203861-539781)x1
Condition: See cases [RCV000510930]
Clinical Significance: uncertain significance
Last Evaluated: 03/10/2016
Review Status: no assertion criteria provided
Related Genes: DOCK8   DOCK8-AS1   KANK1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh379203,861 - 539,781CLINVAR
Cytogenetic Map99p24.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443907
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-01-14
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.