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Variant : CV672686 (GRCh37/hg19 9q21.12(chr9:72519550-73191986)x3) Homo sapiens

Symbol: CV672686
Name: GRCh37/hg19 9q21.12(chr9:72519550-73191986)x3
Condition: not provided [RCV000845802]
Clinical Significance: uncertain significance
Last Evaluated: 06/08/2017
Review Status: no assertion criteria provided
Related Genes: C9orf135   KLF9   MAMDC2   SMC5   TRPM3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37972,519,550 - 73,191,986CLINVAR
Cytogenetic Map99q21.12CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14976260
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-14
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.