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Variant : CV435458 (GRCh37/hg19 6q21(chr6:107662992-108276358)x3) Homo sapiens

Symbol: CV435458
Name: GRCh37/hg19 6q21(chr6:107662992-108276358)x3
Condition: See cases [RCV000512331]
Clinical Significance: uncertain significance
Last Evaluated: 08/10/2015
Review Status: no assertion criteria provided
Related Genes: PDSS2   SCML4   SEC63   SOBP  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh376107,662,992 - 108,276,358CLINVAR
Cytogenetic Map66q21CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13445296
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-12-03
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.