olfml2b[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
nsv6310600	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 161,816,219-162,040,092 , GRCh38.p12 chr1: 161,846,429-162,070,302	OLFML2B, LOC100422526, 2 more genes
nsv3912840	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	OLFML2B, CRB1, 1608 more genes
nsv3873192	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 161,676,893-184,071,723 , GRCh38.p12 chr1: 161,707,103-184,102,589	OLFML2B, COLGALT2, 402 more genes
nsv3889882	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 159,815,642-177,026,983 , GRCh38.p12 chr1: 159,845,852-177,057,847	OLFML2B, FMO4, 403 more genes
nsv4346684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 160,369,890-175,796,325 , GRCh38.p12 chr1: 160,400,100-175,827,189	OLFML2B, LINC00626, 359 more genes
nsv3894431	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 159,977,321-172,200,915 , GRCh37 chr1: 161,710,697-173,934,292 , GRCh38 chr1: 161,740,907-173,965,154	OLFML2B, RPL21P27, 238 more genes
nsv4450412	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 157,321,299-167,391,423 , GRCh38.p12 chr1: 157,351,509-167,422,186	OLFML2B, FCGR3B, 302 more genes
nsv3906717	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 159,479,887-166,895,086 , GRCh37 chr1: 159,449,677-166,864,323 , NCBI36 chr1: 157,716,301-165,130,947	OLFML2B, NOS1AP, 220 more genes
nsv6313604	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 160,417,296-166,197,042 , GRCh38.p12 chr1: 160,447,506-166,227,805	OLFML2B, USF1, 161 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	OLFML2B, MARK1, 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	OLFML2B, SNAP47, 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	OLFML2B, RNU1-153P, 4887 more genes
nsv3918947	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	OLFML2B, LOC101060227, 1608 more genes
nsv3900459	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 149,854,269-180,267,197 , NCBI36 chr1: 148,092,455-178,502,955 , GRCh37 chr1: 149,825,831-180,236,332	OLFML2B, HORMAD1, 923 more genes
nsv3890224	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 157,747,246-176,021,247 , GRCh37 chr1: 157,717,036-175,990,383 , NCBI36 chr1: 155,983,660-174,257,006	OLFML2B, LOC101928596, 475 more genes
nsv6637132	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr1: 161,924,068-164,761,399 , GRCh38.p12 chr1: 161,954,278-164,792,162	OLFML2B, DDR2, 33 more genes
nsv5381285	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699	OLFML2B, DCST1, 2428 more genes
nsv6310595	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr1: 158,581,054-162,750,036 , GRCh38.p12 chr1: 158,611,264-162,780,246	OLFML2B, IGSF8, 193 more genes
nsv4452657	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 160,744,174-162,583,871 , GRCh38.p12 chr1: 160,774,384-162,614,081	OLFML2B, TRD-GTC2-2, 104 more genes
nsv3882809	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 161,469,309-162,517,412 , GRCh38.p12 chr1: 161,499,519-162,547,622	OLFML2B, MIR556, 33 more genes

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Items: 20

Number of Variants: 20

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