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Variant : CV437204 (GRCh37/hg19 15q26.2-26.3(chr15:95136822-102045577)x1) Homo sapiens

Symbol: CV437204
Name: GRCh37/hg19 15q26.2-26.3(chr15:95136822-102045577)x1
Condition: See cases [RCV000512141]
Clinical Significance: pathogenic
Last Evaluated: 09/01/2015
Review Status: no assertion criteria provided
Related Genes: ADAMTS17   ALDH1A3   ARRDC4   ASB7   CERS3   CHSY1   FAM169B   IGF1R   LINS1   LRRC28   LRRK1   LYSMD4   MEF2A   NR2F2   PCSK6   PGPEP1L   SELENOS   SNRPA1   SPATA8   SYNM   TTC23  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000015.9:g.(?_95136822)_(102045577_?)del
Human AssemblyChrPosition (strand)Source
GRCh371595,136,822 - 102,045,577CLINVAR
Cytogenetic Map1515q26.2-26.3CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 13445108
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-08-06
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.