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Variant : CV156304 (GRCh38/hg38 10p15.1-14(chr10:4605831-7403265)x1) Homo sapiens

Symbol: CV156304
Name: GRCh38/hg38 10p15.1-14(chr10:4605831-7403265)x1
Condition: See cases [RCV000135820]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AKR1C1   AKR1C2   AKR1C3   AKR1C4   AKR1E2   ANKRD16   ASB13   CALML3   CALML3-AS1   CALML5   FBH1   GDI2   IL15RA   IL2RA   LASTR   LINC00705   LINC00706   LINC00707   LINC02561   LINC02648   LINC02649   LINC02656   LINC02665   LINC02677   LINC02678   LINP1   LOC106783505   LOC111818965   LOC111946234   LOC111946236   LOC111946241   LOC111946242   LOC111946245   LOC111946246   LOC111946251   LOC116216107   LOC116216108   LOC116216109   LOC116216110   LOC116216111   MANCR   MIR3155A   MIR3155B   NET1   PFKFB3   PRKCQ   PRKCQ-AS1   RBM17   SFMBT2   SNORD129   TASOR2   TRV-TAC3-1   TUBAL3   UCN3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_4605831)_(7403265_?)del
NC_000010.10:g.(?_4648023)_(7445227_?)del
NC_000010.9:g.(?_4638023)_(7485233_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38104,605,831 - 7,403,265CLINVAR
GRCh37104,648,023 - 7,445,227CLINVAR
Build 36104,638,023 - 7,485,233CLINVAR
Cytogenetic Map1010p15.1-14CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483386
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-11-17
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.