acox2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3916461	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960	ACOX2, LOC105377171, 323 more genes
nsv3919181	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 54,045,018-66,060,461 , GRCh37 chr3: 54,079,045-66,046,136 , NCBI36 chr3: 54,054,085-66,021,176	ACOX2, MAGI1-AS1, 135 more genes
nsv4452524	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 57,076,136-65,716,956 , GRCh38.p12 chr3: 57,042,108-65,731,281	ACOX2, LOC105377114, 110 more genes
nsv3875047	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 52,086,599-59,689,209 , GRCh38.p12 chr3: 52,052,583-59,703,483	ACOX2, SLMAP, 132 more genes
nsv3917204	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 57,430,538-64,884,522 , NCBI36 chr3: 57,391,305-64,845,237 , GRCh37 chr3: 57,416,265-64,870,197	ACOX2, C3orf49, 93 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	ACOX2, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	ACOX2, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	ACOX2, RPL23AP49, 2875 more genes
nsv3886371	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 58,089,516-58,799,748 , GRCh38.p12 chr3: 58,103,789-58,814,022	ACOX2, ABHD6, 18 more genes
nsv7097210	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 57,130,421-58,520,833 , GRCh38.p12 chr3: 57,096,393-58,535,106	ACOX2, LOC107984079, 37 more genes
nsv3917956	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 58,495,594-58,651,581 , GRCh37.p13 chr3: 58,520,554-58,676,541 , GRCh38.p12 chr3: 58,534,827-58,690,814	ACOX2, LOC107984079, 4 more genes
nsv4454211	copy number variation	3	nstd102	human	Uncertain significance	GRCh37 chr3: 58,490,107-60,210,773 , GRCh38.p12 chr3: 58,504,380-60,225,045	ACOX2, FAM3D-AS1, 13 more genes
nsv3922342	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 58,459,560-60,177,941 , GRCh37 chr3: 58,484,520-60,202,901 , GRCh38 chr3: 58,498,793-60,217,173	ACOX2, LOC105377112, 14 more genes
nsv6315352	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 58,498,676-60,210,851 , GRCh38.p12 chr3: 58,512,949-60,225,123	ACOX2, CFAP20DC-DT, 12 more genes
nsv3884169	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 58,498,676-60,210,851 , GRCh38.p12 chr3: 58,512,949-60,225,123	ACOX2, FAM107A, 12 more genes
nsv6636568	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 58,498,677-60,210,851 , GRCh38.p12 chr3: 58,512,950-60,225,123	ACOX2, CFAP20DC-DT, 12 more genes
nsv3910870	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr3: 58,534,847-60,199,939 , GRCh37 chr3: 58,520,574-60,185,667 , NCBI36 chr3: 58,495,614-60,160,707	ACOX2, LOC339902, 12 more genes
nsv3918915	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 58,518,554-60,179,169 , NCBI36 chr3: 58,493,594-60,154,209 , GRCh38 chr3: 58,532,827-60,193,441	ACOX2, CFAP20DC-AS1, 12 more genes
nsv3884627	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 58,494,677-60,076,736 , GRCh38.p12 chr3: 58,508,950-60,091,010	ACOX2, CFAP20DC-AS1, 13 more genes

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acox2[All Fields] AND 1[has_clinical] (20)
dbVar
Homo sapiens plexin A2 (PLXNA2), mRNA
Homo sapiens plexin A2 (PLXNA2), mRNA
gi|1519313290|ref|NM_025179.4|

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