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Variant : CV437366 (GRCh37/hg19 7q33(chr7:134379624-135927947)x3) Homo sapiens

Symbol: CV437366
Name: GRCh37/hg19 7q33(chr7:134379624-135927947)x3
Condition: See cases [RCV000511199]
Clinical Significance: uncertain significance
Last Evaluated: 09/09/2015
Review Status: no assertion criteria provided
Related Genes: AGBL3   CALD1   CNOT4   CYREN   FAM180A   LUZP6   MTPN   NUP205   SLC13A4   STMP1   STRA8   TMEM140   WDR91  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh377134,379,624 - 135,927,947CLINVAR
Cytogenetic Map77q33CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 13444174
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-01-21
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.