List of intergenic variants reported as likely benign by GeneDx

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: 31

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HGVS	dbSNP	gnomAD frequency
NC_000003.12:g.49104857C>A	rs192250459	0.00275
GRCh38/hg38 10q26.13(chr10:122751389-122777546)x1
GRCh38/hg38 10q26.2(chr10:126705578-126874970)x1
GRCh38/hg38 12p12.3(chr12:16041251-16088962)x1
GRCh38/hg38 12p12.3(chr12:16041251-16120196)x1
GRCh38/hg38 12q13.11(chr12:47570565-47647966)x4
GRCh38/hg38 13q31.1(chr13:83947821-84116903)x1
GRCh38/hg38 14q21.1(chr14:41378491-41593828)x1
GRCh38/hg38 14q21.1(chr14:42525760-42802470)x1
GRCh38/hg38 14q21.2(chr14:45352239-45510467)x1
GRCh38/hg38 17p11.2(chr17:19601336-19632996)x1
GRCh38/hg38 21q21.3(chr21:27839757-27986029)x1
GRCh38/hg38 2q32.2(chr2:188607058-188721167)x3
GRCh38/hg38 3p22.3(chr3:35472057-35551788)x1
GRCh38/hg38 3p26.3(chr3:427445-462035)x1
GRCh38/hg38 3q13.31(chr3:116718201-116801214)x3
GRCh38/hg38 5q21.3(chr5:105110013-105137553)x1
GRCh38/hg38 6p22.3(chr6:22309428-22390986)x1
GRCh38/hg38 6q16.1(chr6:93778112-93876782)x0
GRCh38/hg38 7p14.3(chr7:32797513-32831789)x3
GRCh38/hg38 7q21.11(chr7:79708363-79763854)x3
GRCh38/hg38 9p22.3(chr9:15310273-15378137)x1
GRCh38/hg38 9p22.3(chr9:15351275-15417031)x1
GRCh38/hg38 Xp22.33(chrX:948314-1152369)x3
GRCh38/hg38 Xq13.2(chrX:73093602-73103636)x2
GRCh38/hg38 Xq22.1(chrX:99445248-99589707)x0
GRCh38/hg38 Xq22.1(chrX:99463846-99589707)x0
GRCh38/hg38 Xq27.3(chrX:145260580-145397053)x0
GRCh38/hg38 Xq28(chrX:149563232-149570094)x1
GRCh38/hg38 Xq28(chrX:155785125-155806648)x1
GRCh38/hg38 Yq11.221(chrY:13988013-13991910)x3

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