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Variant : CV436727 (GRCh37/hg19 4q13.3(chr4:72224764-73824383)x1) Homo sapiens

Symbol: CV436727
Name: GRCh37/hg19 4q13.3(chr4:72224764-73824383)x1
Condition: See cases [RCV000510484]
Clinical Significance: uncertain significance
Last Evaluated: 06/03/2014
Review Status: no assertion criteria provided
Related Genes: ADAMTS3   GC   NPFFR2   SLC4A4  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000004.11:g.(?_72224764)_(73824383_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh37472,224,764 - 73,824,383CLINVAR
Cytogenetic Map44q13.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443463
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-08-06
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.