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Variant : CV73009 (GRCh38/hg38 8p21.2(chr8:24463803-25049184)x3) Homo sapiens

Symbol: CV73009
Name: GRCh38/hg38 8p21.2(chr8:24463803-25049184)x3
Condition: See cases [RCV000052168]
Clinical Significance: uncertain significance
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: AC024958.1   ADAM7   LOC101929294   MIR6841   NEFL   NEFM  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_24463803)_(25049184_?)dup
NC_000008.10:g.(?_24321316)_(24906699_?)dup
NC_000008.9:g.(?_24377206)_(24962616_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38824,463,803 - 25,049,184CLINVAR
GRCh37824,321,316 - 24,906,699CLINVAR
Build 36824,377,206 - 24,962,616CLINVAR
Cytogenetic Map88p21.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8619172
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2020-10-20
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.