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Variant : CV160718 (GRCh38/hg38 7p14.1-13(chr7:42452844-43608265)x3) Homo sapiens

Symbol: CV160718
Name: GRCh38/hg38 7p14.1-13(chr7:42452844-43608265)x3
Condition: See cases [RCV000139756]
Clinical Significance: uncertain significance
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: C7orf25   HECW1   HECW1-IT1   LINC01448   LUARIS   MIR3943   MRPL32   PSMA2   STK17A  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_42452844)_(43608265_?)dup
NC_000007.13:g.(?_42492443)_(43647864_?)dup
NC_000007.12:g.(?_42458968)_(43614389_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38742,452,844 - 43,608,265CLINVAR
GRCh37742,492,443 - 43,647,864CLINVAR
Build 36742,458,968 - 43,614,389CLINVAR
Cytogenetic Map77p14.1-13CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487286
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-11-17
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.