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Variant : CV554815 (GRCh37/hg19 9p24.3(chr9:203861-635302)x3) Homo sapiens

Symbol: CV554815
Name: GRCh37/hg19 9p24.3(chr9:203861-635302)x3
Condition: not provided [RCV000683120]
Clinical Significance: uncertain significance
Last Evaluated: 03/28/2018
Review Status: no assertion criteria provided
Related Genes: DOCK8   DOCK8-AS1   KANK1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh379203,861 - 635,302CLINVAR
Cytogenetic Map99p24.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13796032
Created: 2018-10-09
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.