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Variant : CV162539 (GRCh38/hg38 19p13.12(chr19:15112168-15191333)x1) Homo sapiens

Symbol: CV162539
Name: GRCh38/hg38 19p13.12(chr19:15112168-15191333)x1
Condition: See cases [RCV000141299]
Clinical Significance: uncertain significance
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ILVBL   MIR6795   NOTCH3   SYDE1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000019.10:g.(?_15112168)_(15191333_?)del
NC_000019.9:g.(?_15222979)_(15302144_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381915,112,168 - 15,191,333CLINVAR
GRCh371915,222,979 - 15,302,144CLINVAR
Build 361915,083,979 - 15,163,144CLINVAR
Cytogenetic Map1919p13.12CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9488825
Created: 2014-09-09
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.