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Variant : CV156083 (GRCh38/hg38 Yp11.32-q11.221(chrY:10679-13139461)x0) Homo sapiens

Symbol: CV156083
Name: GRCh38/hg38 Yp11.32-q11.221(chrY:10679-13139461)x0
Condition: See cases [RCV000135637]
Clinical Significance: pathogenic
Last Evaluated: 01/27/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AKAP17A   AMELY   ASMT   ASMTL   ASMTL-AS1   CD99   CRLF2   CSF2RA   DDX3Y   DHRSX   FAM197Y1   FAM197Y2   FAM197Y3   FAM197Y4   FAM197Y5   FAM197Y6   FAM197Y7   FAM197Y8   FAM197Y9   GTPBP6   IL3RA   LINC00102   LINC00106   LINC00278   LINC00279   LINC00280   LINC00685   MIR3690   MIR6089   MIR9985   P2RY8   PCDH11Y   PLCXD1   PPP2R3B   RPS4Y1   SHOX   SLC25A6   SRY   TBL1Y   TGIF2LY   TSPY1   TSPY10   TSPY2   TSPY3   TSPY4   TSPY8   TTTY1   TTTY11   TTTY12   TTTY13B   TTTY15   TTTY16   TTTY18   TTTY19   TTTY1B   TTTY2   TTTY20   TTTY21   TTTY21B   TTTY22   TTTY23   TTTY23B   TTTY2B   TTTY7   TTTY7B   TTTY8   TTTY8B   USP9Y   ZBED1   ZFY   ZFY-AS1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000024.10:g.(?_10679)_(13139461_?)del
NC_000024.9:g.(?_10679)_(15251375_?)del
NC_000024.8:g.(?_679)_(13760769_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38Y10,679 - 13,139,461CLINVAR
GRCh37Y10,679 - 15,251,375CLINVAR
Build 36Y679 - 13,760,769CLINVAR
Cytogenetic MapYYp11.32-q11.221CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483209
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-05-12
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.