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Variant : CV159093 (GRCh38/hg38 2q13(chr2:110104897-110371270)x1) Homo sapiens

Symbol: CV159093
Name: GRCh38/hg38 2q13(chr2:110104897-110371270)x1
Condition: See cases [RCV000138384]
Clinical Significance: benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MALL   MIR4436B2   MTLN   NPHP1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000002.12:g.(?_110104897)_(110371270_?)del
NC_000002.11:g.(?_110862474)_(111128847_?)del
NC_000002.10:g.(?_110219763)_(110563384_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh382110,104,897 - 110,371,270CLINVAR
GRCh372110,862,474 - 111,128,847CLINVAR
Build 362110,219,763 - 110,563,384CLINVAR
Cytogenetic Map22q13CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485933
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.