ClinVar Miner

Variants studied for chromosome Y disorder

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign association total
4 3 7 0 0 1 15

Gene and significance breakdown #

Total genes and gene combinations: 10
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Gene or gene combination pathogenic likely pathogenic uncertain significance association total
USP9Y 1 0 3 0 4
​intergenic 0 0 2 0 2
CFTR 1 1 0 0 2
FAM83F 0 0 1 0 1
HOXD13 1 0 0 0 1
KIF3B 0 0 0 1 1
LOC108281134, SOX3 0 0 1 0 1
MSH4 1 0 0 0 1
PNLDC1 0 1 0 0 1
TBC1D25 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 9
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Submitter pathogenic likely pathogenic uncertain significance association total
Clinical Bioinformatic Lab, Royan Institute 1 1 0 1 3
Revvity Omics, Revvity 0 0 2 0 2
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 0 0 2 0 2
Talkowski Laboratory, Center for Human Genetic Research, Massachusetts General Hospital 0 0 2 0 2
Institute of Human Genetics, University Hospital Muenster 1 1 0 0 2
OMIM 1 0 0 0 1
Centre for Mendelian Genomics, University Medical Centre Ljubljana 1 0 0 0 1
Zotz-Klimas Genetics Lab, MVZ Zotz Klimas 0 0 1 0 1
Center for Genetics and Inherited Diseases, Taibah University 0 1 0 0 1

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