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Variant : CV555662 (GRCh37/hg19 17q25.3(chr17:80243845-80374899)x1) Homo sapiens

Symbol: CV555662
Name: GRCh37/hg19 17q25.3(chr17:80243845-80374899)x1
Condition: not provided [RCV000683967]
Clinical Significance: likely benign
Last Evaluated: 08/24/2017
Review Status: no assertion criteria provided
Related Genes: CD7   OGFOD3   SECTM1   TEX19   UTS2R  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371780,243,845 - 80,374,899CLINVAR
Cytogenetic Map1717q25.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798061
Created: 2018-10-09
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.