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Variant : CV157496 (GRCh38/hg38 19p13.12(chr19:14406909-15410770)x1) Homo sapiens

Symbol: CV157496
Name: GRCh38/hg38 19p13.12(chr19:14406909-15410770)x1
Condition: See cases [RCV000136896]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADGRE2   ADGRE3   ADGRE5   AKAP8   AKAP8L   BRD4   CASP14   CCDC105   CLEC17A   DDX39A   DNAJB1   EPHX3   GIPC1   ILVBL   MIR639   MIR6795   NDUFB7   NOTCH3   OR1I1   OR7A10   OR7A17   OR7A5   OR7C1   OR7C2   PKN1   PTGER1   SLC1A6   SNORA104   SYDE1   TECR   ZNF333  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000019.10:g.(?_14406909)_(15410770_?)del
NC_000019.9:g.(?_14517721)_(15521581_?)del
NC_000019.8:g.(?_14378721)_(15382581_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381914,406,909 - 15,410,770CLINVAR
GRCh371914,517,721 - 15,521,581CLINVAR
Build 361914,378,721 - 15,382,581CLINVAR
Cytogenetic Map1919p13.12CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9484457
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.