List of intergenic variants reported as pathogenic for not provided

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
GRCh37/hg19 1q31.1(chr1:188620903-188928487)x1
GRCh37/hg19 1q31.1-31.2(chr1:190622633-191184941)x1
GRCh37/hg19 9q12(chr9:55958158-55978098)x1
GRCh37/hg19 Xp22.33(chrX:168546-1234634)x1
GRCh37/hg19 Xp22.33(chrX:168546-1358900)x1
GRCh37/hg19 Xp22.33(chrX:168546-1411818)x1
GRCh37/hg19 Xp22.33(chrX:168546-1616945)x1
GRCh37/hg19 Xp22.33(chrX:168546-1734397)x1
GRCh37/hg19 Xp22.33(chrX:168546-1922907)x0
GRCh37/hg19 Xp22.33(chrX:168546-781139)x1
GRCh37/hg19 Xp22.33(chrX:168547-1536716)x1
GRCh37/hg19 Xp22.33(chrX:168547-2057937)x1
GRCh37/hg19 Xp22.33(chrX:217329-1234634)x1
GRCh37/hg19 Xp22.33(chrX:310147-1734397)x1
GRCh37/hg19 Xp22.33(chrX:356281-2382269)x1
GRCh37/hg19 Xp22.33(chrX:416347-756010)x1
GRCh37/hg19 Xp22.33(chrX:450823-862460)x1
GRCh37/hg19 Xp22.33(chrX:450941-1651464)x1
GRCh37/hg19 Xp22.33(chrX:450941-827222)x1
GRCh37/hg19 Xp22.33(chrX:482532-1460944)x1
GRCh37/hg19 Xp22.33(chrX:502307-1234634)x1
GRCh37/hg19 Xp22.33(chrX:502858-837407)x1
GRCh37/hg19 Xp22.33(chrX:534390-935361)x1
GRCh37/hg19 Xp22.33(chrX:546305-650199)x1
GRCh37/hg19 Xp22.33(chrX:585079-619564)x3
GRCh37/hg19 Xp22.33(chrX:602793-629993)x1
GRCh37/hg19 Xp22.33(chrX:614727-636490)x0
GRCh37/hg19 Xq25(chrX:123244958-123406369)x3
GRCh37/hg19 Yq11.23-12(chrY:28792268-58883690)x0
NC_000001.11:g.231487317_231487320del	rs527236214
Single allele

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