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Variant : CV248447 (GRCh37/hg19 9q34.11(chr9:131550680-131775355)x3) Homo sapiens

Symbol: CV248447
Name: GRCh37/hg19 9q34.11(chr9:131550680-131775355)x3
Condition: See cases [RCV000240044]
Clinical Significance: uncertain significance
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: DOLK   ENDOG   KYAT1   LRRC8A   NUP188   PHYHD1   SH3GLB2   SPOUT1   TBC1D13  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh379131,550,680 - 131,775,355CLINVAR
Cytogenetic Map99q34.11CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11541508
Created: 2016-10-11
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.