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Variant : CV354201 (GRCh37/hg19 14q23.1(chr14:58737402-58884615)x1) Homo sapiens

Symbol: CV354201
Name: GRCh37/hg19 14q23.1(chr14:58737402-58884615)x1
Condition: Thyroid Hemiagenesis [RCV000488902]|Thyroid hemiagenesis [RCV000488902]
Clinical Significance: pathogenic|likely pathogenic
Last Evaluated: 08/31/2016
Review Status: no assertion criteria provided
Related Genes: ARID4A   PSMA3   TIMM9   TOMM20L  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing|research
Position
Human AssemblyChrPosition (strand)Source
GRCh371458,737,402 - 58,884,615CLINVAR
Cytogenetic Map1414q23.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12905434
Created: 2017-06-06
Species: Homo sapiens
Last Modified: 2019-11-12
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.