oxr1[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3910348	copy number variation	1	nstd102	human	Benign	NCBI36 chr8: 107,376,988-107,739,178 , GRCh37 chr8: 107,307,812-107,670,002 , GRCh38 chr8: 106,295,584-106,657,774	OXR1, OXR1-AS1
nsv3908081	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 107,535,798-107,546,500 , GRCh38.p12 chr8: 106,523,570-106,534,272	OXR1, OXR1-AS1
nsv3908577	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 107,509,850-107,773,415 , GRCh38.p12 chr8: 106,497,622-106,761,187	OXR1, TAGLN2P1, 3 more genes
nsv3901450	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 107,032,887-120,742,018 , GRCh38.p12 chr8: 106,020,659-119,729,778	OXR1, AARD, 112 more genes
nsv3922470	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 102,183,491-110,139,893 , GRCh38 chr8: 101,171,263-109,127,664 , NCBI36 chr8: 102,252,667-110,209,069	OXR1, HMGB1P46, 109 more genes
nsv3913241	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 101,260,812-107,606,071 , GRCh38 chr8: 100,179,408-106,524,667 , GRCh37 chr8: 101,191,636-107,536,895	OXR1, LRP12, 113 more genes
nsv3919996	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 102,897,047-108,368,371 , GRCh38 chr8: 101,884,819-107,356,143 , NCBI36 chr8: 102,966,223-108,437,547	OXR1, BAALC-AS1, 79 more genes
nsv3891425	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 28,623,965-33,361,042 , GRCh37 chr1: 28,751,378-33,588,455 , GRCh38 chr1: 28,424,867-33,122,854	SNHG3, LOC105378620, 115 more genes
nsv3914089	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 106,065,758-108,815,763 , GRCh38 chr8: 105,053,530-107,803,535 , NCBI36 chr8: 106,134,934-108,884,939	OXR1, ANGPT1, 16 more genes
nsv3895257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 31,239,605-33,825,029 , NCBI36 chr1: 31,012,192-33,597,616 , GRCh38 chr1: 30,766,758-33,359,428	LOC105378623, TINAGL1, 85 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	MARK1, LINC02766, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	SNAP47, STK40, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	RNU1-153P, MIR3917, 4887 more genes
nsv3915173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636	OXR1, RN7SL474P, 2109 more genes
nsv3901821	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028	OXR1, TBC1D31, 2109 more genes
nsv4349554	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385	OXR1, LOC101929488, 2105 more genes
nsv3916777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575	OXR1, RPL5P22, 2105 more genes
nsv3898123	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385	OXR1, SPAG1, 2105 more genes
nsv3908608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028	OXR1, LINC01617, 2105 more genes
nsv3893757	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442	OXR1, LOC105375890, 2105 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 62

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Number of Variants: 20

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