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Variant : CV158564 (GRCh38/hg38 8p21.3-21.2(chr8:22946697-25125997)x3) Homo sapiens

Symbol: CV158564
Name: GRCh38/hg38 8p21.3-21.2(chr8:22946697-25125997)x3
Condition: See cases [RCV000137878]
Clinical Significance: uncertain significance
Last Evaluated: 10/21/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC024958.1   AC090197.1   AC100861.1   AC107959.4   ADAM28   ADAM7   ADAMDEC1   CHMP7   ENTPD4   LOC101929294   LOC111255642   LOC111255645   LOC113788270   LOC113788271   LOC113788272   LOC114827823   LOC116186924   LOXL2   MIR6841   NEFL   NEFM   NKX2-6   NKX3-1   R3HCC1   RHOBTB2   SLC25A37   STC1   TNFRSF10A   TNFRSF10B   TNFRSF10C   TNFRSF10D  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_22946697)_(25125997_?)dup
NC_000008.10:g.(?_22804210)_(24983512_?)dup
NC_000008.9:g.(?_22860155)_(25039429_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38822,946,697 - 25,125,997CLINVAR
GRCh37822,804,210 - 24,983,512CLINVAR
Build 36822,860,155 - 25,039,429CLINVAR
Cytogenetic Map88p21.3-21.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485429
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-10-20
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.