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Variant : CV155194 (GRCh38/hg38 2q13(chr2:110025674-110321488)x3) Homo sapiens

Symbol: CV155194
Name: GRCh38/hg38 2q13(chr2:110025674-110321488)x3
Condition: See cases [RCV000134815]
Clinical Significance: benign
Last Evaluated: 10/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MALL   MIR4267   MIR4436B1   MIR4436B2   MTLN   NPHP1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000002.12:g.(?_110025674)_(110321488_?)dup
NC_000002.11:g.(?_110783251)_(111079065_?)dup
NC_000002.10:g.(?_110140540)_(110513563_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh382110,025,674 - 110,321,488CLINVAR
GRCh372110,783,251 - 111,079,065CLINVAR
Build 362110,140,540 - 110,513,563CLINVAR
Cytogenetic Map22q13CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482392
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.