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Variant : CV155535 (GRCh38/hg38 15q26.3(chr15:98010889-98142484)x1) Homo sapiens

Symbol: CV155535
Name: GRCh38/hg38 15q26.3(chr15:98010889-98142484)x1
Condition: See cases [RCV000135110]
Clinical Significance: benign
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC01582   LINC02251  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_98010889)_(98142484_?)del
NC_000015.9:g.(?_98554119)_(98685713_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381598,010,889 - 98,142,484CLINVAR
GRCh371598,554,119 - 98,685,713CLINVAR
Build 361596,371,582 - 96,503,236CLINVAR
Cytogenetic Map1515q26.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9482683
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-10-08
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.