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Variant : CV162432 (GRCh38/hg38 1q44(chr1:248250956-248787141)x3) Homo sapiens

Symbol: CV162432
Name: GRCh38/hg38 1q44(chr1:248250956-248787141)x3
Condition: See cases [RCV000141214]
Clinical Significance: benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LYPD8   OR14C36   OR14I1   OR2G6   OR2M7   OR2T1   OR2T10   OR2T11   OR2T12   OR2T2   OR2T27   OR2T29   OR2T3   OR2T33   OR2T34   OR2T35   OR2T4   OR2T5   OR2T6   OR2T7  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000001.11:g.(?_248250956)_(248787141_?)dup
NC_000001.10:g.(?_248414258)_(249081340_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381248,250,956 - 248,787,141CLINVAR
GRCh371248,414,258 - 249,081,340CLINVAR
Build 361246,480,881 - 247,047,963CLINVAR
Cytogenetic Map11q44CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9488741
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-07
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.