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Variant : CV435928 (GRCh37/hg19 1p36.22-36.21(chr1:11143298-13709344)x3) Homo sapiens

Symbol: CV435928
Name: GRCh37/hg19 1p36.22-36.21(chr1:11143298-13709344)x3
Condition: See cases [RCV000510407]
Clinical Significance: uncertain significance
Last Evaluated: 12/14/2014
Review Status: no assertion criteria provided
Related Genes: AADACL3   AADACL4   AGTRAP   ANGPTL7   C1orf158   C1orf167   CLCN6   DHRS3   DISP3   DRAXIN   EXOSC10   FBXO2   FBXO44   FBXO6   HNRNPCL1   HNRNPCL2   KIAA2013   MAD2L2   MFN2   MIIP   MTHFR   MTOR   NPPA   NPPB   PLOD1   PRAMEF1   PRAMEF10   PRAMEF11   PRAMEF12   PRAMEF13   PRAMEF15   PRAMEF18   PRAMEF19   PRAMEF2   PRAMEF22   PRAMEF4   PRAMEF5   PRAMEF6   PRAMEF7   PRAMEF8   PRAMEF9   TNFRSF1B   TNFRSF8   UBIAD1   VPS13D  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37111,143,298 - 13,709,344CLINVAR
Cytogenetic Map11p36.22-36.21CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443386
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-01-21
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.