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Variant : CV157383 (GRCh38/hg38 19q13.33(chr19:49623273-49747363)x3) Homo sapiens

Symbol: CV157383
Name: GRCh38/hg38 19q13.33(chr19:49623273-49747363)x3
Condition: See cases [RCV000136795]
Clinical Significance: benign
Last Evaluated: 10/01/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADM5   BCL2L12   CPT1C   IRF3   MIR5088   PRMT1   PRR12   RRAS   SCAF1   TSKS  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000019.10:g.(?_49623273)_(49747363_?)dup
NC_000019.9:g.(?_50126530)_(50250620_?)dup
NC_000019.8:g.(?_54818342)_(54942432_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381949,623,273 - 49,747,363CLINVAR
GRCh371950,126,530 - 50,250,620CLINVAR
Build 361954,818,342 - 54,942,432CLINVAR
Cytogenetic Map1919q13.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9484356
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.