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Variant : CV382013 (GRCh37/hg19 1p35.3(chr1:28666901-28929761)x3) Homo sapiens

Symbol: CV382013
Name: GRCh37/hg19 1p35.3(chr1:28666901-28929761)x3
Condition: See cases [RCV000448758]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: PHACTR4   RAB42   RCC1   SNHG3   SNORA73A   TAF12   TRNAU1AP  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37128,666,901 - 28,929,761CLINVAR
Cytogenetic Map11p35.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12853459
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-02-20
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.