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Variant : CV159707 (GRCh38/hg38 7q11.23(chr7:73755813-74133404)x3) Homo sapiens

Symbol: CV159707
Name: GRCh38/hg38 7q11.23(chr7:73755813-74133404)x3
Condition: See cases [RCV000138886]
Clinical Significance: uncertain significance
Last Evaluated: 10/24/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CLDN3   CLDN4   ELN   LIMK1   METTL27   TMEM270  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_73755813)_(74133404_?)dup
NW_003871064.1:g.(?_1285049)_(1662640_?)dup
NC_000007.12:g.(?_72808079)_(73185670_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38773,755,813 - 74,133,404CLINVAR
Build 36772,808,079 - 73,185,670CLINVAR
Cytogenetic Map77q11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9486419
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
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.