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Variant : CV162461 (GRCh38/hg38 3q12.1(chr3:99941846-100170010)x1) Homo sapiens

Symbol: CV162461
Name: GRCh38/hg38 3q12.1(chr3:99941846-100170010)x1
Condition: See cases [RCV000141235]
Clinical Significance: likely benign
Last Evaluated: 12/10/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CMSS1   FILIP1L   MIR3921  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_99941846)_(100170010_?)del
NC_000003.11:g.(?_99660690)_(99888854_?)del
NC_000003.10:g.(?_101143380)_(101371544_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38399,941,846 - 100,170,010CLINVAR
GRCh37399,660,690 - 99,888,854CLINVAR
Build 363101,143,380 - 101,371,544CLINVAR
Cytogenetic Map33q12.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9488762
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-28
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.