riox2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3882713	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 97,631,081-97,736,465 , GRCh38.p12 chr3: 97,912,237-98,017,621	RIOX2, GABRR3, 1 more genes
nsv3918176	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 99,026,548-99,209,616 , GRCh37.p13 chr3: 97,543,858-97,726,926 , GRCh38.p12 chr3: 97,825,014-98,008,082	RIOX2, LOC105373994, 2 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	RIOX2, NECTIN3, 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	RIOX2, MTCO2P29, 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	RIOX2, ATP6V1A, 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	RIOX2, ZBTB11-AS1, 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	RIOX2, RNU4-62P, 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	RIOX2, NDUFB4, 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	RIOX2, RPL23AP49, 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	RIOX2, OR7E53P, 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	RIOX2, COL8A1, 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	RIOX2, AKR1B1P2, 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	RIOX2, COL8A1, 132 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	RIOX2, LOC105373998, 33 more genes
nsv4673879	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 96,850,456-97,974,150 , GRCh38.p12 chr3: 97,131,612-98,255,306	RIOX2, OR5BM1P, 22 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	RIOX2, LOC105373997, 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	RIOX2, OR5H4P, 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	RIOX2, OR5AC4P, 25 more genes
nsv6636342	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 97,377,527-97,805,568 , GRCh38.p12 chr3: 97,658,683-98,086,724	RIOX2, EPHA6, 8 more genes

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