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Variant : CV162789 (GRCh38/hg38 Yq11.223-11.23(chrY:23127722-24882383)x0) Homo sapiens

Symbol: CV162789
Name: GRCh38/hg38 Yq11.223-11.23(chrY:23127722-24882383)x0
Condition: See cases [RCV000141537]
Clinical Significance: likely benign
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: BPY2B   CDY1B   DAZ1   DAZ2   DAZ3   DAZ4   TTTY17B   TTTY3B   TTTY4B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_23127722)_(24882383_?)del
NC_000024.9:g.(?_25273869)_(27028530_?)del
NC_000024.8:g.(?_23683257)_(25437918_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38Y23,127,722 - 24,882,383CLINVAR
GRCh37Y25,273,869 - 27,028,530CLINVAR
Build 36Y23,683,257 - 25,437,918CLINVAR
Cytogenetic MapYYq11.223-11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489062
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-20
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.