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Variant : CV170822 (GRCh38/hg38 8p23.1(chr8:12182421-12610034)x1) Homo sapiens

Symbol: CV170822
Name: GRCh38/hg38 8p23.1(chr8:12182421-12610034)x1
Condition: See cases [RCV000148201]
Clinical Significance: benign
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: AC068587.4   DEFB130A   FAM66A   FAM85A   FAM86B1   FAM86B2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_12182421)_(12610034_?)del
NC_000008.10:g.(?_12039930)_(12467543_?)del
NC_000008.9:g.(?_12077339)_(12511914_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38812,182,421 - 12,610,034CLINVAR
GRCh37812,039,930 - 12,467,543CLINVAR
Build 36812,077,339 - 12,511,914CLINVAR
Cytogenetic Map88p23.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9684750
Created: 2014-12-09
Species: Homo sapiens
Last Modified: 2020-06-30
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.