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Variant : CV161424 (GRCh38/hg38 5p15.33-15.32(chr5:3057457-4922388)x1) Homo sapiens

Symbol: CV161424
Name: GRCh38/hg38 5p15.33-15.32(chr5:3057457-4922388)x1
Condition: See cases [RCV000140377]
Clinical Significance: uncertain significance
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: IRX1   LINC01017   LINC01019   LINC01377   LINC02063   LINC02114   LINC02162  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000005.10:g.(?_3057457)_(4922388_?)del
NC_000005.9:g.(?_3057571)_(4922501_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3853,057,457 - 4,922,388CLINVAR
GRCh3753,057,571 - 4,922,501CLINVAR
Build 3653,110,571 - 4,975,501CLINVAR
Cytogenetic Map55p15.33-15.32CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487907
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-20
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.