List of intergenic variants reported as uncertain significance for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 21

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 10p14(chr10:10875814-10962054)x1
GRCh37/hg19 11p14.2(chr11:26166090-26245567)x1
GRCh37/hg19 11p14.2(chr11:26167420-26245567)x1
GRCh37/hg19 12q14.3(chr12:67123301-67579538)x1
GRCh37/hg19 1p31.1(chr1:82134940-82242495)x3
GRCh37/hg19 3q25.2(chr3:154374528-154778328)x1
GRCh37/hg19 5q15(chr5:92828411-92911270)
GRCh37/hg19 6q25.1(chr6:149471775-149619493)x1
GRCh37/hg19 7q36.2(chr7:153778741-154268709)x3
GRCh37/hg19 7q36.2(chr7:153939110-154012649)x1
GRCh37/hg19 Xp22.33(chrX:2885808-2906380)
GRCh37/hg19 Xp22.33(chrX:562054-1358900)
GRCh37/hg19 Xp22.33(chrX:727225-2042258)
GRCh37/hg19 Xp22.33(chrX:878066-1411818)
GRCh37/hg19 Xp22.33(chrX:986336-2129785)
t(10;14)(p14;q24)dn
t(15;16)(q24;p13)dn
t(1;14)(q25;q11)dn
t(2;14)(p11.2;q11.2)dn
t(6;18)(q14.1;q21.1)dn
t(9;21)(p21;q22)dn

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