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Variant : CV164863 (GRCh38/hg38 15q26.2-26.3(chr15:97681713-101920998)x1) Homo sapiens

Symbol: CV164863
Name: GRCh38/hg38 15q26.2-26.3(chr15:97681713-101920998)x1
Condition: See cases [RCV000143176]
Clinical Significance: pathogenic
Last Evaluated: 12/10/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADAMTS17   ALDH1A3   ARRDC4   ASB7   CERS3   CERS3-AS1   CHSY1   FAM169B   IGF1R   IRAIN   LINC00923   LINC01582   LINC02244   LINC02251   LINC02348   LINC02351   LINS1   LRRC28   LRRK1   LUNAR1   LYSMD4   MEF2A   MIR4714   OR4F15   OR4F6   PCSK6   PCSK6-AS1   PGPEP1L   SELENOS   SNRPA1   SPATA41   SYNM   TARSL2   TM2D3   TTC23  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_97681713)_(101920998_?)del
NC_000015.9:g.(?_98224943)_(102461201_?)del
NC_000015.8:g.(?_96025947)_(100278724_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381597,681,713 - 101,920,998CLINVAR
GRCh371598,224,943 - 102,461,201CLINVAR
Build 361596,025,947 - 100,278,724CLINVAR
Cytogenetic Map1515q26.2-26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9490774
Created: 2014-09-09
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.