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Variant : CV156405 (GRCh38/hg38 1p36.13(chr1:16621632-16905322)x1) Homo sapiens

Symbol: CV156405
Name: GRCh38/hg38 1p36.13(chr1:16621632-16905322)x1
Condition: See cases [RCV000135910]
Clinical Significance: benign
Last Evaluated: 10/14/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MIR3675   MST1L   RNU1-2   RNU1-3   RNU1-4   TRE-TTC3-1   TRG-CCC1-2   TRG-CCC4-1   TRG-CCC5-1   TRN-GTT13-1   TRN-GTT4-1   TRQ-CTG14-1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000001.11:g.(?_16621632)_(16905322_?)del
NC_000001.10:g.(?_16948127)_(17231817_?)del
NC_000001.9:g.(?_16820714)_(17104404_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38116,621,632 - 16,905,322CLINVAR
GRCh37116,948,127 - 17,231,817CLINVAR
Build 36116,820,714 - 17,104,404CLINVAR
Cytogenetic Map11p36.13CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483476
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-31
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.