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Variant : CV155178 (GRCh38/hg38 17q25.1(chr17:73851718-74610906)x3) Homo sapiens

Symbol: CV155178
Name: GRCh38/hg38 17q25.1(chr17:73851718-74610906)x3
Condition: See cases [RCV000134803]
Clinical Significance: benign
Last Evaluated: 09/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: BTBD17   C17orf77   CD300A   CD300C   CD300E   CD300H   CD300LB   CD300LD   DNAI2   GPR142   GPRC5C   KIF19   LINC02074   RPL38   TTYH2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000017.11:g.(?_73851718)_(74610906_?)dup
NC_000017.10:g.(?_71847857)_(72607045_?)dup
NC_000017.9:g.(?_69359452)_(70118640_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381773,851,718 - 74,610,906CLINVAR
GRCh371771,847,857 - 72,607,045CLINVAR
Build 361769,359,452 - 70,118,640CLINVAR
Cytogenetic Map1717q25.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482380
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.