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Variant : CV73008 (GRCh38/hg38 8p21.2(chr8:23961808-25436108)x3) Homo sapiens

Symbol: CV73008
Name: GRCh38/hg38 8p21.2(chr8:23961808-25436108)x3
Condition: See cases [RCV000052167]
Clinical Significance: uncertain significance
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: AC024958.1   ADAM28   ADAM7   ADAMDEC1   DOCK5   GNRH1   KCTD9   LOC101929294   LOC105379331   LOC113788272   LOC113788273   LOC113788274   MIR6841   MIR6876   NEFL   NEFM  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_23961808)_(25436108_?)dup
NC_000008.10:g.(?_23819321)_(25293624_?)dup
NC_000008.9:g.(?_23875266)_(25349541_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38823,961,808 - 25,436,108CLINVAR
GRCh37823,819,321 - 25,293,624CLINVAR
Build 36823,875,266 - 25,349,541CLINVAR
Cytogenetic Map88p21.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8619171
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2020-10-15
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.