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Variant : CV594362 (GRCh37/hg19 17q25.1(chr17:71834001-72690918)x3) Homo sapiens

Symbol: CV594362
Name: GRCh37/hg19 17q25.1(chr17:71834001-72690918)x3
Condition: not provided [RCV000739662]
Clinical Significance: uncertain significance
Last Evaluated: 04/04/2012
Review Status: no assertion criteria provided
Related Genes: BTBD17   C17orf77   CD300A   CD300C   CD300E   CD300LB   CD300LD   CD300LF   DNAI2   GPR142   GPRC5C   KIF19   RAB37   RPL38   TTYH2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371771,834,001 - 72,690,918CLINVAR
Cytogenetic Map1717q25.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14355036
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-03-24
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.