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Variant : CV161221 (GRCh38/hg38 19q13.2(chr19:39010191-39035118)x1) Homo sapiens

Symbol: CV161221
Name: GRCh38/hg38 19q13.2(chr19:39010191-39035118)x1
Condition: See cases [RCV000140183]
Clinical Significance: uncertain significance
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: FBXO27  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000019.10:g.(?_39010191)_(39035118_?)del
NC_000019.9:g.(?_39500831)_(39525758_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381939,010,191 - 39,035,118CLINVAR
GRCh371939,500,831 - 39,525,758CLINVAR
Build 361944,192,671 - 44,217,598CLINVAR
Cytogenetic Map1919q13.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487713
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-30
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.