acox1[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
nsv6137857	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 73,937,119-73,956,296 , GRCh38.p12 chr17: 75,941,038-75,960,215	ACOX1
nsv6310238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 73,951,637-73,956,466 , GRCh38.p12 chr17: 75,955,556-75,960,385	ACOX1
nsv4682241	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 73,942,819-73,953,657 , GRCh38.p12 chr17: 75,946,738-75,957,576	ACOX1
nsv5673054	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 73,944,322-73,944,548 , GRCh38.p12 chr17: 75,948,241-75,948,467	ACOX1
nsv4683206	copy number variation	2	nstd102	human	Pathogenic, Likely pathogenic	GRCh37 chr17: 73,956,286-73,956,466 , GRCh38.p12 chr17: 75,960,205-75,960,385	ACOX1
nsv7094988	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 73,942,829-73,956,476 , GRCh38.p12 chr17: 75,946,748-75,960,395	ACOX1
nsv7095418	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 73,942,829-73,953,667 , GRCh38.p12 chr17: 75,946,748-75,957,586	ACOX1
nsv3908048	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr17: 73,929,152-73,955,205 , GRCh38.p12 chr17: 75,933,071-75,959,124	ACOX1, FBF1
nsv4769393	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 73,926,095-73,949,575 , GRCh38.p12 chr17: 75,930,014-75,953,494	ACOX1, FBF1
nsv6137863	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 73,937,588-73,974,614 , GRCh38.p12 chr17: 75,941,507-75,978,533	ACOX1, TEN1, 1 more genes
nsv3886451	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 73,969,686-73,975,174 , GRCh38 chr17: 75,973,605-75,979,093	ACOX1, TEN1, 1 more genes
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	ACOX1, PRPSAP1, 1350 more genes
nsv3919795	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 71,144,026-71,478,420 , GRCh37 chr17: 73,632,431-73,966,825 , GRCh38 chr17: 75,636,351-75,970,744	ACOX1, ITGB4, 15 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	ACOX1, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	ACOX1, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	ACOX1, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	ACOX1, SMURF2, 2366 more genes
nsv3914783	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577	ACOX1, LOC105371922, 1855 more genes
nsv3909511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846	ACOX1, FOXK2, 958 more genes
nsv4457646	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062	ACOX1, LOC107985089, 448 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 33

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Number of Variants: 20

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