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Variant : CV156683 (GRCh38/hg38 1q44(chr1:248176668-248406116)x3) Homo sapiens

Symbol: CV156683
Name: GRCh38/hg38 1q44(chr1:248176668-248406116)x3
Condition: See cases [RCV000136153]
Clinical Significance: benign
Last Evaluated: 02/06/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: OR14C36   OR2M2   OR2M3   OR2M4   OR2M7   OR2T1   OR2T12   OR2T33   OR2T4   OR2T6  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000001.11:g.(?_248176668)_(248406116_?)dup
NC_000001.10:g.(?_248339970)_(248569417_?)dup
NC_000001.9:g.(?_246406593)_(246636040_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381248,176,668 - 248,406,116CLINVAR
GRCh371248,339,970 - 248,569,417CLINVAR
Build 361246,406,593 - 246,636,040CLINVAR
Cytogenetic Map11q44CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483714
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.