or1a1[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
nsv3904164	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 3,098,544-3,119,767 , GRCh38.p12 chr17: 3,195,250-3,216,473	OR1A1, OR1A2
nsv3913013	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055	OR1A1, RPS4XP17, 289 more genes
nsv3915884	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 45,835-6,862,369 , GRCh38 chr17: 162,088-6,959,050 , NCBI36 chr17: 11,879-6,803,093	OR1A1, LOC105371592, 222 more genes
nsv3922546	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 525-5,779,421 , GRCh38 chr17: 150,732-5,935,377 , GRCh37 chr17: 525-5,838,697	OR1A1, CHRNE, 198 more genes
nsv4674912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088	OR1A1, SRR, 196 more genes
nsv3913795	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 43,098-5,496,266 , GRCh37 chr17: 45,835-5,555,542 , GRCh38 chr17: 193,307-5,652,222	OR1A1, BHLHA9, 194 more genes
nsv3921779	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 87,039-4,585,577 , GRCh38 chr17: 237,248-4,735,533 , GRCh37 chr17: 396,627-4,638,828	OR1A1, ARRB2, 146 more genes
nsv3919819	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 50,690-4,168,935 , NCBI36 chr17: 48,539-4,115,684 , GRCh38 chr17: 198,748-4,265,640	OR1A1, LOC105371430, 125 more genes
nsv3904699	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-3,871,323 , GRCh38.p12 chr17: 157,423-3,968,029	OR1A1, OVCA2, 120 more genes
nsv3892866	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-3,825,428 , GRCh38.p12 chr17: 150,732-3,922,134	OR1A1, OR1P1, 120 more genes
nsv3920266	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 226,472-3,655,099 , NCBI36 chr17: 76,263-3,505,142 , GRCh37 chr17: 396,627-3,558,393	OR1A1, RN7SL624P, 107 more genes
nsv3902288	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 48,858-3,379,400 , GRCh38.p12 chr17: 199,067-3,476,106	OR1A1, GEMIN4, 100 more genes
nsv3920795	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 2,062,380-5,258,340 , NCBI36 chr17: 1,912,424-5,102,359 , GRCh37 chr17: 1,965,674-5,161,635	OR1A1, LINC01996, 128 more genes
nsv3913766	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 150,732-3,242,868 , NCBI36 chr17: 525-3,092,912 , GRCh37 chr17: 525-3,146,162	OR1A1, LOC105371483, 90 more genes
nsv3892504	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 2,050,166-4,315,506 , GRCh38.p12 chr17: 2,146,872-4,412,211	OR1A1, OR3A2, 73 more genes
nsv6112772	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 2,313,096-3,735,525 , GRCh38.p12 chr17: 2,409,802-3,832,231	OR1A1, LOC105371592, 49 more genes
nsv6310130	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 2,541,583-3,819,519 , GRCh38.p12 chr17: 2,638,289-3,916,225	OR1A1, ASPA, 46 more genes
nsv3894473	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 2,339,561-3,447,162 , GRCh38.p12 chr17: 2,436,267-3,543,868	OR1A1, LOC105371592, 34 more genes
nsv3919228	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 2,377,554-3,317,209 , GRCh37 chr17: 2,430,804-3,370,459 , GRCh38 chr17: 2,527,510-3,467,165	OR1A1, OR3A3, 31 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	OR1A1, MIR3185, 2366 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 54

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Number of Variants: 20

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