OR5H2 - 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
nsv4586840	copy number variation	1	nstd183	human		GRCh37 chr3: 97,998,756-98,001,588 , GRCh38.p12 chr3: 98,279,912-98,282,744	OR5H2, LOC105373999
nsv3971284	copy number variation	1	nstd168	human		GRCh38 chr3: 98,270,844-98,313,096 , GRCh37.p13 chr3: 97,989,688-98,031,940	OR5H8, OR5H2, 1 more genes
nsv7148201	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857	NECTIN3, H2BP3, 418 more genes
nsv3918661	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683	MTCO2P29, GAP43, 401 more genes
nsv3917160	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,021,157-118,088,593 , GRCh38 chr3: 93,819,623-116,887,056 , GRCh37 chr3: 93,538,467-116,605,903	ATP6V1A, RPS10P4, 297 more genes
nsv3910775	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 97,514,213-115,382,196 , GRCh38 chr3: 97,795,369-115,663,349 , NCBI36 chr3: 98,996,903-116,864,886	ZBTB11-AS1, RABGGTBP1, 258 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	RNU4-62P, SEMA3B-AS1, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	NDUFB4, LOC105374108, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	RPL23AP49, DLEC1, 2875 more genes
nsv3922717	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168	OR7E53P, HSPA8P9, 794 more genes
nsv4728581	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 95,563,096-102,371,126 , GRCh38.p12 chr3: 95,844,252-102,652,282	COL8A1, CPOX, 107 more genes
nsv6314751	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 72,488,757-99,614,758 , GRCh38.p12 chr3: 72,439,606-99,895,914	AKR1B1P2, COL8A1, 231 more genes
nsv3911724	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr3: 95,021,157-105,090,283 , GRCh37 chr3: 93,538,467-103,607,593 , GRCh38 chr3: 93,819,623-103,888,749	COL8A1, CPOX, 132 more genes
nsv3918930	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 97,742,604-98,051,633 , GRCh38 chr3: 98,023,760-98,332,789 , NCBI36 chr3: 99,225,294-99,534,323	OR5H4P, OR5BM1P, 19 more genes
nsv4674270	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 97,994,048-98,260,542 , GRCh38.p12 chr3: 98,275,204-98,541,698	RPL38P4, OR5K1, 10 more genes
nsv3874747	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 96,579,273-98,216,225 , GRCh38.p12 chr3: 96,860,429-98,497,381	LOC105373998, OR5H14, 33 more genes
nsv6636842	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 97,283,117-98,218,677 , GRCh38.p12 chr3: 97,564,273-98,499,833	LOC105373997, LOC105374000, 31 more genes
nsv4674762	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 97,606,054-98,499,715 , GRCh38.p12 chr3: 97,887,210-98,780,871	OR5H4P, LOC105373999, 36 more genes
nsv3873905	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 97,650,137-98,174,233 , GRCh38.p12 chr3: 97,931,293-98,455,389	OR5AC4P, LOC105373996, 25 more genes
esv4007705	copy number variation	1	estd231	human		GRCh37 chr3: 97,754,744-98,109,449 , GRCh38.p12 chr3: 98,035,900-98,390,605	OR5H1, OR5H8, 21 more genes

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Organism

Variant Type

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Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 106

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Number of Variants: 20

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