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Variant : CV158360 (GRCh38/hg38 1q44(chr1:245805927-246647918)x3) Homo sapiens

Symbol: CV158360
Name: GRCh38/hg38 1q44(chr1:245805927-246647918)x3
Condition: See cases [RCV000137679]
Clinical Significance: uncertain significance
Last Evaluated: 08/29/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CNST   LINC01743   LOC110121251   SMYD3   SMYD3-AS1   TFB2M  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000001.11:g.(?_245805927)_(246647918_?)dup
NC_000001.10:g.(?_245969229)_(246811220_?)dup
NC_000001.9:g.(?_244035852)_(244877843_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381245,805,927 - 246,647,918CLINVAR
GRCh371245,969,229 - 246,811,220CLINVAR
Build 361244,035,852 - 244,877,843CLINVAR
Cytogenetic Map11q44CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485231
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-09-29
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.