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Variant : CV73030 (GRCh38/hg38 8q24.3(chr8:144392063-144458958)x3) Homo sapiens

Symbol: CV73030
Name: GRCh38/hg38 8q24.3(chr8:144392063-144458958)x3
Condition: See cases [RCV000052189]
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: ADCK5   CPSF1   CYHR1   MIR1234   MIR6849   MIR6893   MIR939   SLC39A4   TONSL   TONSL-AS1   VPS28  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_144392063)_(144458958_?)dup
NC_000008.10:g.(?_145617263)_(145684341_?)dup
NC_000008.9:g.(?_145588071)_(145655149_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh388144,392,063 - 144,458,958CLINVAR
GRCh378145,617,263 - 145,684,341CLINVAR
Build 368145,588,071 - 145,655,149CLINVAR
Cytogenetic Map88q24.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8619193
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2020-05-26
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.