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Variant : CV156789 (GRCh38/hg38 1p36.21(chr1:12779298-13075120)x1) Homo sapiens

Symbol: CV156789
Name: GRCh38/hg38 1p36.21(chr1:12779298-13075120)x1
Condition: See cases [RCV000136259]
Clinical Significance: benign
Last Evaluated: 03/08/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: HNRNPCL1   HNRNPCL3   LINC01784   PRAMEF1   PRAMEF10   PRAMEF11   PRAMEF2   PRAMEF25   PRAMEF27   PRAMEF4   PRAMEF6   PRAMEF7  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000001.11:g.(?_12779298)_(13075120_?)del
NC_000001.10:g.(?_12839441)_(13142569_?)del
NC_000001.9:g.(?_12762028)_(13065156_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38112,779,298 - 13,075,120CLINVAR
GRCh37112,839,441 - 13,142,569CLINVAR
Build 36112,762,028 - 13,065,156CLINVAR
Cytogenetic Map11p36.21CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483820
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-07
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.