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Variant : CV158768 (GRCh38/hg38 15q11.2(chr15:24897997-25103626)x3) Homo sapiens

Symbol: CV158768
Name: GRCh38/hg38 15q11.2(chr15:24897997-25103626)x3
Condition: See cases [RCV000138077]
Clinical Significance: uncertain significance
Last Evaluated: 01/10/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: PWAR5   PWAR6   PWARSN   SNHG14   SNORD107   SNORD108   SNORD109A   SNORD116-1   SNORD116-10   SNORD116-11   SNORD116-12   SNORD116-13   SNORD116-14   SNORD116-15   SNORD116-16   SNORD116-17   SNORD116-18   SNORD116-19   SNORD116-2   SNORD116-20   SNORD116-21   SNORD116-22   SNORD116-23   SNORD116-24   SNORD116-25   SNORD116-26   SNORD116-27   SNORD116-3   SNORD116-4   SNORD116-5   SNORD116-6   SNORD116-7   SNORD116-8   SNORD116-9   SNORD116@   SNORD64   SNRPN   SNURF  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_24897997)_(25103626_?)dup
NC_000015.9:g.(?_25143144)_(25348773_?)dup
NC_000015.8:g.(?_22694237)_(22899866_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381524,897,997 - 25,103,626CLINVAR
GRCh371525,143,144 - 25,348,773CLINVAR
Build 361522,694,237 - 22,899,866CLINVAR
Cytogenetic Map1515q11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485626
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-21
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.