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Variant : CV155894 (GRCh38/hg38 1p36.22-36.21(chr1:12293275-13111197)x3) Homo sapiens

Symbol: CV155894
Name: GRCh38/hg38 1p36.22-36.21(chr1:12293275-13111197)x3
Condition: See cases [RCV000135466]
Clinical Significance: benign
Last Evaluated: 07/30/2009
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AADACL3   AADACL4   C1orf158   DHRS3   HNRNPCL1   HNRNPCL3   LINC01784   LINC02766   MIR6730   PRAMEF1   PRAMEF10   PRAMEF11   PRAMEF12   PRAMEF2   PRAMEF25   PRAMEF27   PRAMEF4   PRAMEF6   PRAMEF7   SNORA59A   VPS13D  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000001.11:g.(?_12293275)_(13111197_?)dup
NC_000001.10:g.(?_12353332)_(13178669_?)dup
NC_000001.9:g.(?_12275919)_(13101256_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38112,293,275 - 13,111,197CLINVAR
GRCh37112,353,332 - 13,178,669CLINVAR
Build 36112,275,919 - 13,101,256CLINVAR
Cytogenetic Map11p36.22-36.21CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483039
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.