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Variant : CV158191 (GRCh38/hg38 17p13.2(chr17:4141725-4778120)x1) Homo sapiens

Symbol: CV158191
Name: GRCh38/hg38 17p13.2(chr17:4141725-4778120)x1
Condition: See cases [RCV000137514]
Clinical Significance: uncertain significance
Last Evaluated: 02/18/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC091153.3   ALOX15   ANKFY1   ARRB2   CXCL16   CYB5D2   GGT6   LINC01996   MED11   MYBBP1A   PELP1   SMTNL2   SPNS2   SPNS3   TM4SF5   UBE2G1   ZMYND15   ZZEF1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000017.11:g.(?_4141725)_(4778120_?)del
NC_000017.10:g.(?_4045019)_(4681415_?)del
NC_000017.9:g.(?_3991768)_(4628164_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38174,141,725 - 4,778,120CLINVAR
GRCh37174,045,019 - 4,681,415CLINVAR
Build 36173,991,768 - 4,628,164CLINVAR
Cytogenetic Map1717p13.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9485069
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-23
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.