ClinVar Miner

List of variants reported as likely pathogenic by Clinical Cytogenomics Laboratory,Center for Precision Diagnostics, University of Washington

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Total variants: 16
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GRCh37/hg19 16p13.11(chr16:14968859-16291983)x3
GRCh37/hg19 16p13.11-12.3(chr16:15499057-18264837)x4
GRCh37/hg19 1p34.2(chr1:41343608-43121507)x1
GRCh37/hg19 1q21.1(chr1:145416056-146089268)x3
GRCh37/hg19 20p11.22-11.21(chr20:21680345-24383453)x1
GRCh37/hg19 22q11.21(chr22:21062566-21463730)x1
GRCh37/hg19 22q11.22-11.23(chr22:22989304-23666474)x1
GRCh37/hg19 2q11.1-11.2(chr2:96747466-98193473)x1
GRCh37/hg19 2q23.1(chr2:148942537-149035397)x1
GRCh37/hg19 3p13(chr3:71129956-71255015)x1
GRCh37/hg19 4q24(chr4:101953182-102026137)x1
GRCh37/hg19 4q31.23(chr4:149135444-149320303)x3
GRCh37/hg19 7p22.1(chr7:4644965-5436368)x3
GRCh37/hg19 Xp22.31(chrX:6179830-8605251)x2
GRCh37/hg19 Xp22.31(chrX:6596639-8135053)x3
GRCh37/hg19 Xq28(chrX:154256858-154297348)x0

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