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Variant : CV156750 (GRCh38/hg38 16p13.3(chr16:521803-558532)x1) Homo sapiens

Symbol: CV156750
Name: GRCh38/hg38 16p13.3(chr16:521803-558532)x1
Condition: See cases [RCV000136220]
Clinical Significance: benign
Last Evaluated: 02/06/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CAPN15   LINC00235   MIR3176   MIR5587   RAB11FIP3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000016.10:g.(?_521803)_(558532_?)del
NC_000016.9:g.(?_571803)_(608532_?)del
NC_000016.8:g.(?_511804)_(548533_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3816521,803 - 558,532CLINVAR
GRCh3716571,803 - 608,532CLINVAR
Build 3616511,804 - 548,533CLINVAR
Cytogenetic Map1616p13.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9483781
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
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.