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Variant : CV157781 (GRCh38/hg38 13q12.11-12.12(chr13:21164677-22802191)x3) Homo sapiens

Symbol: CV157781
Name: GRCh38/hg38 13q12.11-12.12(chr13:21164677-22802191)x3
Condition: See cases [RCV000137123]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: FGF9   LINC00424   LINC00539   LINC00540   LINC01046   MICU2   MRPL57   SKA3   ZDHHC20  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000013.11:g.(?_21164677)_(22802191_?)dup
NC_000013.10:g.(?_21738816)_(23376330_?)dup
NC_000013.9:g.(?_20636816)_(22274330_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381321,164,677 - 22,802,191CLINVAR
GRCh371321,738,816 - 23,376,330CLINVAR
Build 361320,636,816 - 22,274,330CLINVAR
Cytogenetic Map1313q12.11-12.12CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9484682
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-07
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.