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Variant : CV382732 (GRCh37/hg19 15q26.2-26.3(chr15:94782891-102429112)x1) Homo sapiens

Symbol: CV382732
Name: GRCh37/hg19 15q26.2-26.3(chr15:94782891-102429112)x1
Condition: See cases [RCV000445764]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ADAMTS17   ALDH1A3   ARRDC4   ASB7   CERS3   CHSY1   FAM169B   IGF1R   LINS1   LRRC28   LRRK1   LYSMD4   MCTP2   MEF2A   NR2F2   OR4F15   OR4F6   PCSK6   PGPEP1L   SELENOS   SNRPA1   SPATA8   SYNM   TARSL2   TM2D3   TTC23  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.9:g.(?_94782891)_(102429112_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh371594,782,891 - 102,429,112CLINVAR
Cytogenetic Map1515q26.2-26.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12850497
Created: 2017-04-11
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.