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Variant : CV156185 (GRCh38/hg38 7q21.3(chr7:93410151-93604672)x1) Homo sapiens

Symbol: CV156185
Name: GRCh38/hg38 7q21.3(chr7:93410151-93604672)x1
Condition: See cases [RCV000135731]|See cases [RCV000149543]
Clinical Significance: uncertain significance
Last Evaluated: 05/06/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CALCR   MIR489   MIR653  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_93410151)_(93604672_?)del
NC_000007.13:g.(?_93039463)_(93233984_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38793,410,151 - 93,604,672CLINVAR
GRCh37793,039,463 - 93,233,984CLINVAR
Build 36792,877,399 - 93,071,920CLINVAR
Cytogenetic Map77q21.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483299
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-11-05
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.