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Variant : CV436648 (GRCh37/hg19 1p36.31(chr1:5962543-6062001)x4) Homo sapiens

Symbol: CV436648
Name: GRCh37/hg19 1p36.31(chr1:5962543-6062001)x4
Condition: See cases [RCV000511414]
Clinical Significance: uncertain significance
Last Evaluated: 08/27/2015
Review Status: no assertion criteria provided
Related Genes: KCNAB2   NPHP4  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3715,962,543 - 6,062,001CLINVAR
Cytogenetic Map11p36.31CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13444386
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.