or5v1[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
nsv3874366	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 29,335,537-29,352,943 , GRCh38.p12 chr6: 29,367,760-29,385,166	OR5V1, OR12D3
nsv3875319	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 29,406,696-29,412,162 , GRCh38.p12 chr6: 29,438,919-29,444,385	OR5V1, OR10C1, 1 more genes
nsv3873680	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 29,406,696-29,408,554 , GRCh38.p12 chr6: 29,438,919-29,440,777	OR5V1, LOC105379641, 1 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	OR5V1, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	OR5V1, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	OR5V1, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	OR5V1, ITPR3, 2905 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	OR5V1, TRR-ACG1-2, 1385 more genes
nsv3920564	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946	OR5V1, PRELID1P2, 785 more genes
nsv6289880	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 28,005,012-31,683,185 , GRCh38.p12 chr6: 28,037,234-31,715,408	OR5V1, ABCF1, 313 more genes
nsv3921531	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr6: 29,030,671-29,433,996 , GRCh37 chr6: 28,922,692-29,326,017 , GRCh38 chr6: 28,954,915-29,358,240	OR5V1, OR2J4P, 28 more genes
nsv3874405	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 28,920,972-29,354,383 , GRCh38.p12 chr6: 28,953,195-29,386,606	OR5V1, OR2B3, 30 more genes
nsv3887063	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 28,920,972-29,348,297 , GRCh38.p12 chr6: 28,953,195-29,380,520	OR5V1, OR2B3, 30 more genes
nsv3919878	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr6: 29,030,676-29,434,066 , GRCh38 chr6: 28,954,920-29,358,310 , GRCh37 chr6: 28,922,697-29,326,087	OR5V1, OR2B3, 28 more genes
nsv3888352	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 28,735,761-29,585,573 , GRCh38.p12 chr6: 28,767,984-29,617,796	OR5V1, OR12D1, 75 more genes
nsv3921510	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 29,407,237-29,556,283 , GRCh37.p13 chr6: 29,299,258-29,448,304 , GRCh38.p12 chr6: 29,331,481-29,480,527	OR5V1, OR11A1, 10 more genes
nsv3870570	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 28,130,359-32,108,367 , GRCh38.p12 chr6: 28,162,581-32,140,590	OR5V1, LOC105375002, 345 more genes
nsv6636314	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 29,162,783-30,236,331 , GRCh38.p12 chr6: 29,195,006-30,268,554	OR5V1, LOC353009, 92 more genes
nsv3912336	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 28,730,964-29,737,605 , GRCh38 chr6: 28,763,187-29,769,828 , NCBI36 chr6: 28,838,943-29,845,584	OR5V1, OR2AD1P, 87 more genes
nsv3918042	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 28,987,399-29,465,533 , GRCh37.p13 chr6\|NT_167245.1: 245,961-622,457 , GRCh37.p13 chr6\|NT_167247.1: 186,758-635,908 , GRCh37.p13 chr6\|NT_167249.1: 233,223-673,240 , GRCh37.p13 chr6\|NT_167246.1: 184,244-635,721 , GRCh37.p13 chr6: 28,879,420-29,357,554 , GRCh38.p12 chr6: 28,911,643-29,389,777 , GRCh38.p12 chr6\|NT_167247.2: 181,174-630,323 , GRCh38.p12 chr6\|NT_167249.2: 233,925-673,942 , GRCh38.p12 chr6\|NT_167245.2: 240,377-616,872 , GRCh38.p12 chr6\|NT_167246.2: 178,625-630,101	OR5V1, ZNF311, 38 more genes

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Items: 20

Number of Variants: 20

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