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Variant : CV161398 (GRCh38/hg38 16q24.2-24.3(chr16:88662702-88719577)x1) Homo sapiens

Symbol: CV161398
Name: GRCh38/hg38 16q24.2-24.3(chr16:88662702-88719577)x1
Condition: See cases [RCV000140351]
Clinical Significance: benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CTU2   MIR4722   MVD   PIEZO1   RNF166   SNAI3   SNAI3-AS1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000016.10:g.(?_88662702)_(88719577_?)del
NC_000016.9:g.(?_88729110)_(88785985_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381688,662,702 - 88,719,577CLINVAR
GRCh371688,729,110 - 88,785,985CLINVAR
Build 361687,256,611 - 87,313,486CLINVAR
Cytogenetic Map1616q24.2-24.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487881
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.