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Variant : CV604143 (GRCh37/hg19 1q44(chr1:248071583-248843314)x3) Homo sapiens

Symbol: CV604143
Name: GRCh37/hg19 1q44(chr1:248071583-248843314)x3
Condition: not provided [RCV000749443]
Clinical Significance: benign
Last Evaluated: 10/16/2013
Review Status: no assertion criteria provided
Related Genes: OR14C36   OR2AK2   OR2G6   OR2L13   OR2L2   OR2L3   OR2L5   OR2L8   OR2M2   OR2M3   OR2M4   OR2M5   OR2M7   OR2T1   OR2T10   OR2T11   OR2T12   OR2T2   OR2T27   OR2T29   OR2T3   OR2T33   OR2T34   OR2T35   OR2T4   OR2T5   OR2T6   OR2T8  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371248,071,583 - 248,843,314CLINVAR
Cytogenetic Map11q44CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14364772
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-06-23
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.