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Variant : CV159214 (GRCh38/hg38 Xp11.4(chrX:37955473-38120350)x3) Homo sapiens

Symbol: CV159214
Name: GRCh38/hg38 Xp11.4(chrX:37955473-38120350)x3
Condition: See cases [RCV000138478]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: H2AP   MIR548AJ2   SYTL5  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_37955473)_(38120350_?)dup
NC_000023.10:g.(?_37814726)_(37979603_?)dup
NC_000023.9:g.(?_37699670)_(37864547_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X37,955,473 - 38,120,350CLINVAR
GRCh37X37,814,726 - 37,979,603CLINVAR
Build 36X37,699,670 - 37,864,547CLINVAR
Cytogenetic MapXXp11.4CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486020
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-17
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.