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Variant : CV155929 (GRCh38/hg38 2q13(chr2:110104900-110611314)x1) Homo sapiens

Symbol: CV155929
Name: GRCh38/hg38 2q13(chr2:110104900-110611314)x1
Condition: See cases [RCV000135500]
Clinical Significance: benign
Last Evaluated: 10/19/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LIMS4   LINC01106   MALL   MIR4436B2   MTLN   NPHP1   RGPD6  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000002.12:g.(?_110104900)_(110611314_?)del
NC_000002.11:g.(?_110862477)_(111368891_?)del
NC_000002.10:g.(?_110219766)_(111085360_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh382110,104,900 - 110,611,314CLINVAR
GRCh372110,862,477 - 111,368,891CLINVAR
Build 362110,219,766 - 111,085,360CLINVAR
Cytogenetic Map22q13CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483073
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-31
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.