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Variant : CV156419 (GRCh38/hg38 1p36.13(chr1:16615158-16905322)x3) Homo sapiens

Symbol: CV156419
Name: GRCh38/hg38 1p36.13(chr1:16615158-16905322)x3
Condition: See cases [RCV000135921]
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 gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000001.11:g.(?_16615158)_(16905322_?)dup
NC_000001.10:g.(?_16941653)_(17231817_?)dup
NC_000001.9:g.(?_16814240)_(17104404_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38116,615,158 - 16,905,322CLINVAR
GRCh37116,941,653 - 17,231,817CLINVAR
Build 36116,814,240 - 17,104,404CLINVAR
Cytogenetic Map11p36.13CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483487
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.