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Variant : CV156289 (GRCh38/hg38 7q11.21(chr7:65039567-65804880)x1) Homo sapiens

Symbol: CV156289
Name: GRCh38/hg38 7q11.21(chr7:65039567-65804880)x1
Condition: See cases [RCV000135810]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LOC441242   SNORA15B-1   SNORA15B-2   SNORA22   SNORA22C   ZNF92  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_65039567)_(65804880_?)del
NC_000007.13:g.(?_64499945)_(65208605_?)del
NC_000007.12:g.(?_64137380)_(64907302_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38765,039,567 - 65,804,880CLINVAR
GRCh37764,499,945 - 65,208,605 (+)CLINVAR
Build 36764,137,380 - 64,907,302CLINVAR
Cytogenetic Map77q11.21CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483376
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.