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Variant : CV674034 (GRCh37/hg19 4p16.1(chr4:8162995-8481259)x1) Homo sapiens

Symbol: CV674034
Name: GRCh37/hg19 4p16.1(chr4:8162995-8481259)x1
Condition: not provided [RCV000847150]
Clinical Significance: uncertain significance
Last Evaluated: 12/27/2017
Review Status: no assertion criteria provided
Related Genes: ACOX3   HTRA3   SH3TC1   TRMT44  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3748,162,995 - 8,481,259CLINVAR
Cytogenetic Map44p16.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14977731
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-09-29
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.