or5l1[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
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	OR5L1, FAUP4, 2031 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	OR5L1, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	OR5L1, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	OR5L1, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	OR5L1, PYGM, 2125 more genes
nsv6315474	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199	OR5L1, TRR-TCT3-2, 494 more genes
nsv3911150	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 55,086,995-58,766,250 , NCBI36 chr11: 54,843,571-58,522,826 , GRCh38 chr11: 55,319,519-58,998,777	OR5L1, OR5BD1P, 197 more genes
nsv3924455	copy number variation	1	nstd102	human	Benign	GRCh38 chr11: 55,445,689-57,114,783 , GRCh37 chr11: 55,213,165-56,882,257 , NCBI36 chr11: 54,969,741-56,638,833	OR5L1, OR5AL1, 111 more genes
nsv3896950	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 54,697,347-56,021,284 , GRCh38.p12 chr11: 54,929,872-56,253,808	OR5L1, OR5D15P, 66 more genes
nsv3902541	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 54,794,237-56,003,589 , GRCh38.p12 chr11: 55,026,761-56,236,113	OR5L1, OR5J1P, 65 more genes
nsv3920198	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr11: 54,807,338-55,776,171 , GRCh37.p13 chr11: 55,050,762-56,019,595 , GRCh38.p12 chr11: 55,283,286-56,252,119	OR5L1, OR5F2P, 65 more genes
nsv3910165	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 55,033,261-55,997,702 , GRCh38 chr11: 55,265,785-56,230,226 , NCBI36 chr11: 54,789,837-55,754,278	OR5L1, OR5D18, 65 more genes
nsv3902131	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 55,029,738-55,980,347 , GRCh38.p12 chr11: 55,262,262-56,212,871	OR5L1, OR8I2, 64 more genes
nsv3895805	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 55,033,164-55,980,347 , GRCh38.p12 chr11: 55,265,688-56,212,871	OR5L1, OR5D2P, 64 more genes
nsv3916926	copy number variation	2	nstd102	human	Benign	GRCh37 chr11: 55,086,995-55,980,406 , GRCh38 chr11: 55,319,519-56,212,930 , NCBI36 chr11: 54,843,571-55,736,982	OR5L1, OR4A15, 61 more genes
nsv3924382	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr11: 55,316,591-55,855,055 , GRCh37 chr11: 55,084,067-55,622,531 , NCBI36 chr11: 54,840,643-55,379,107	OR5L1, OR5L2, 31 more genes
nsv3904152	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 49,313,405-59,008,426 , GRCh38.p12 chr11: 49,291,853-59,240,953	OR5L1, FAM111B, 250 more genes
nsv4453292	copy number variation	1	nstd102	human	not provided	GRCh37 chr11: 55,033,164-57,518,726 , GRCh38.p12 chr11: 55,265,688-57,751,254	OR5L1, OR8J3, 150 more genes
nsv3924646	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 55,316,535-57,539,457 , GRCh37 chr11: 55,084,011-57,306,930 , NCBI36 chr11: 54,840,587-57,063,506	OR5L1, OR5AL1, 134 more genes
nsv3918615	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr11: 54,789,872-56,896,303 , GRCh37.p13 chr11: 55,033,296-57,139,727 , GRCh38.p12 chr11: 55,265,820-57,372,254	OR5L1, OR8K5, 127 more genes

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Items: 20

Number of Variants: 20

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