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Variant : CV158495 (GRCh38/hg38 9p24.1-23(chr9:7406754-10757763)x1) Homo sapiens

Symbol: CV158495
Name: GRCh38/hg38 9p24.1-23(chr9:7406754-10757763)x1
Condition: See cases [RCV000137810]
Clinical Significance: uncertain significance
Last Evaluated: 09/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AL513422.1   DMAC1   PTPRD   PTPRD-AS1   PTPRD-AS2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000009.12:g.(?_7406754)_(10757763_?)del
NC_000009.11:g.(?_7406754)_(10757763_?)del
NC_000009.10:g.(?_7396754)_(10747763_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3897,406,754 - 10,757,763CLINVAR
GRCh3797,406,754 - 10,757,763CLINVAR
Build 3697,396,754 - 10,747,763CLINVAR
Cytogenetic Map99p24.1-23CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9485362
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-30
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.