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Variant : CV155723 (GRCh38/hg38 Yq11.223-11.23(chrY:21927773-26133012)x0) Homo sapiens

Symbol: CV155723
Name: GRCh38/hg38 Yq11.223-11.23(chrY:21927773-26133012)x0
Condition: See cases [RCV000135298]
Clinical Significance: pathogenic
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: BPY2   BPY2B   BPY2C   CDY1   CDY1B   DAZ1   DAZ2   DAZ3   DAZ4   PRY   PRY2   RBMY1F   RBMY1J   TTTY17A   TTTY17B   TTTY17C   TTTY3   TTTY3B   TTTY4   TTTY4B   TTTY4C   TTTY5   TTTY6   TTTY6B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_21927773)_(26133012_?)del
NC_000024.9:g.(?_24073920)_(28279159_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38Y21,927,773 - 26,133,012CLINVAR
GRCh37Y24,073,920 - 28,279,159CLINVAR
Build 36Y22,483,308 - 26,688,547CLINVAR
Cytogenetic MapYYq11.223-11.23CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482871
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-11
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.