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Variant : CV155114 (GRCh38/hg38 1q44(chr1:248176671-248400557)x1) Homo sapiens

Symbol: CV155114
Name: GRCh38/hg38 1q44(chr1:248176671-248400557)x1
Condition: See cases [RCV000134753]
Clinical Significance: benign
Last Evaluated: 07/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: OR14C36   OR2M2   OR2M3   OR2M4   OR2M7   OR2T12   OR2T33   OR2T4   OR2T6  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000001.11:g.(?_248176671)_(248400557_?)del
NC_000001.10:g.(?_248339973)_(248563858_?)del
NC_000001.9:g.(?_246406596)_(246630481_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381248,176,671 - 248,400,557CLINVAR
GRCh371248,339,973 - 248,563,858CLINVAR
Build 361246,406,596 - 246,630,481CLINVAR
Cytogenetic Map11q44CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482331
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.