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Variant : CV674878 (GRCh37/hg19 3q29(chr3:195573221-196124278)x3) Homo sapiens

Symbol: CV674878
Name: GRCh37/hg19 3q29(chr3:195573221-196124278)x3
Condition: not provided [RCV000847985]
Clinical Significance: uncertain significance
Last Evaluated: 07/31/2017
Review Status: no assertion criteria provided
Related Genes: PCYT1A   SLC51A   TCTEX1D2   TFRC   TM4SF19   TNK2   TNK2-AS1   UBXN7   ZDHHC19  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh373195,573,221 - 196,124,278CLINVAR
Cytogenetic Map33q29CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14979558
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-03-17
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.