List of variants reported as uncertain significance for See cases by Cytogenetics Laboratory, University of Washington

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 34

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 11p11.2(chr11:47310499-47351543)x3
GRCh37/hg19 11q13.1(chr11:64485197-64691737)x3
GRCh37/hg19 16p12.2(chr16:21601904-21739542)x1
GRCh37/hg19 16p13.3(chr16:6344789-6673241)x3
GRCh37/hg19 17p13.3(chr17:789447-969524)x3
GRCh37/hg19 19p13.3(chr19:823554-1206859)x3
GRCh37/hg19 20p12.1(chr20:16730002-17286002)x3
GRCh37/hg19 21q22.3(chr21:43749126-43904643)x1
GRCh37/hg19 21q22.3(chr21:47486134-47796810)x3
GRCh37/hg19 22q11.22(chr22:22320654-22566334)x1
GRCh37/hg19 2p12(chr2:77354773-78176219)x3
GRCh37/hg19 3p13(chr3:73524387-73613399)x1
GRCh37/hg19 3p26.3(chr3:2291018-2781213)x3
GRCh37/hg19 3p26.3-26.2(chr3:2214694-2812860)x1
GRCh37/hg19 3q29(chr3:197127599-197771083)x3
GRCh37/hg19 4p15.32-15.31(chr4:16830399-17805183)x3
GRCh37/hg19 5q15(chr5:92919336-92925582)x4
GRCh37/hg19 5q21.1(chr5:98241365-98339090)x3
GRCh37/hg19 5q35.3(chr5:180096438-180217003)x3
GRCh37/hg19 6p24.3-24.2(chr6:10490144-10724301)x1
GRCh37/hg19 6q26(chr6:162519220-162710973)x1
GRCh37/hg19 6q26(chr6:162780748-163001030)x1
GRCh37/hg19 8p22(chr8:15249009-16017680)x1
GRCh37/hg19 8q24.3(chr8:145600952-145834119)x3
GRCh37/hg19 9p22.1(chr9:19354041-19548029)x3
GRCh37/hg19 9q31.1(chr9:107972883-108105377)x3
GRCh37/hg19 Xp11.4(chrX:38485991-38626762)x3
GRCh37/hg19 Xp22.2(chrX:11541839-12655449)x3
GRCh37/hg19 Xp22.31(chrX:6118522-6405679)x3
GRCh37/hg19 Xp22.31(chrX:6776818-7119738)x3
GRCh37/hg19 Xp22.31(chrX:7050418-7247772)x3
GRCh37/hg19 Xp22.31(chrX:7449660-8150511)x2
GRCh37/hg19 Xq11.2(chrX:63131115-63414996)x2
GRCh37/hg19 Xq26.2(chrX:131885089-132500236)x2

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