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Variant : CV157929 (GRCh38/hg38 10p15.1(chr10:4871826-5811361)x3) Homo sapiens

Symbol: CV157929
Name: GRCh38/hg38 10p15.1(chr10:4871826-5811361)x3
Condition: See cases [RCV000137253]
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   ASB13   CALML3   CALML3-AS1   CALML5   GDI2   LASTR   LINC02561   LINC02677   LINC02678   LOC111946236   LOC111946241   LOC111946242   LOC116216108   LOC116216109   LOC116216110   LOC116216111   NET1   TASOR2   TUBAL3   UCN3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_4871826)_(5811361_?)dup
NC_000010.10:g.(?_4914018)_(5853324_?)dup
NC_000010.9:g.(?_4904018)_(5893330_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38104,871,826 - 5,811,361CLINVAR
GRCh37104,914,018 - 5,853,324CLINVAR
Build 36104,904,018 - 5,893,330CLINVAR
Cytogenetic Map1010p15.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9484811
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.