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Variant : CV674717 (GRCh37/hg19 16p13.3(chr16:5107989-5186447)x1) Homo sapiens

Symbol: CV674717
Name: GRCh37/hg19 16p13.3(chr16:5107989-5186447)x1
Condition: not provided [RCV000847831]
Clinical Significance: uncertain significance
Last Evaluated: 04/24/2017
Review Status: no assertion criteria provided
Related Genes: ALG1   C16orf89   EEF2KMT  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37165,107,989 - 5,186,447CLINVAR
Cytogenetic Map1616p13.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14979367
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.