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Variant : CV554142 (GRCh37/hg19 4q26(chr4:115565977-115890735)x3) Homo sapiens

Symbol: CV554142
Name: GRCh37/hg19 4q26(chr4:115565977-115890735)x3
Condition: not provided [RCV000682447]
Clinical Significance: uncertain significance
Last Evaluated: 03/10/2018
Review Status: no assertion criteria provided
Related Genes: NDST4   UGT8  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh374115,565,977 - 115,890,735CLINVAR
Cytogenetic Map44q26CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13795332
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-01-21
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.