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Variant : CV554053 (GRCh37/hg19 3q29(chr3:195891339-196137752)x1) Homo sapiens

Symbol: CV554053
Name: GRCh37/hg19 3q29(chr3:195891339-196137752)x1
Condition: not provided [RCV000682358]
Clinical Significance: uncertain significance
Last Evaluated: 11/14/2017
Review Status: no assertion criteria provided
Related Genes: PCYT1A   SLC51A   TCTEX1D2   TM4SF19   UBXN7   ZDHHC19  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh373195,891,339 - 196,137,752CLINVAR
Cytogenetic Map33q29CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13795241
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-03-31
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.