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Variant : CV156398 (GRCh38/hg38 1p36.21(chr1:12800662-12858960)x1) Homo sapiens

Symbol: CV156398
Name: GRCh38/hg38 1p36.21(chr1:12800662-12858960)x1
Condition: See cases [RCV000135904]
Clinical Significance: benign
Last Evaluated: 10/14/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: HNRNPCL1   LINC01784   PRAMEF11   PRAMEF2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000001.11:g.(?_12800662)_(12858960_?)del
NC_000001.10:g.(?_12860810)_(12918815_?)del
NC_000001.9:g.(?_12783397)_(12841402_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38112,800,662 - 12,858,960CLINVAR
GRCh37112,860,810 - 12,918,815CLINVAR
Build 36112,783,397 - 12,841,402CLINVAR
Cytogenetic Map11p36.21CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483470
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-21
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.