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Variant : CV156947 (GRCh38/hg38 2q13(chr2:110025681-110576905)x1) Homo sapiens

Symbol: CV156947
Name: GRCh38/hg38 2q13(chr2:110025681-110576905)x1
Condition: See cases [RCV000136417]
Clinical Significance: benign
Last Evaluated: 03/08/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LIMS4   LINC01106   MALL   MIR4267   MIR4436B1   MIR4436B2   MTLN   NPHP1   RGPD6  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000002.12:g.(?_110025681)_(110576905_?)del
NC_000002.11:g.(?_110783258)_(111334482_?)del
NC_000002.10:g.(?_110140547)_(110811832_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh382110,025,681 - 110,576,905 (+)CLINVAR
GRCh372110,783,258 - 111,334,482 (+)CLINVAR
Build 362110,140,547 - 110,811,832CLINVAR
Cytogenetic Map22q13CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483978
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.