cis-1-Bromo-1-butene - 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
nsv4090595	copy number variation	1	nstd166	human		GRCh37.p13 chr3: 50,635,948-50,643,247 , GRCh38.p12 chr3: 50,598,517-50,605,816	CISH
nsv4079550	copy number variation	1	nstd166	human		GRCh37.p13 chr3: 50,642,122-50,643,672 , GRCh38.p12 chr3: 50,604,691-50,606,241	CISH
nsv3912778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 49,498,433-55,348,528 , GRCh38 chr3: 49,461,000-55,314,500 , NCBI36 chr3: 49,473,437-55,323,568	SEMA3G, INKA1, 160 more genes
nsv4728146	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 48,807,193-51,363,558 , GRCh38.p12 chr3: 48,769,760-51,326,127	APEH, MIR5193, 90 more genes
nsv6311990	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 49,547,968-50,685,477 , GRCh38.p12 chr3: 49,510,535-50,648,046	APEH, RNA5SP131, 52 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	RNU4-62P, SEMA3B-AS1, 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	NDUFB4, LOC105374108, 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	RPL23AP49, DLEC1, 2875 more genes
nsv4347762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589	UQCRC1, DHX30, 291 more genes
nsv3921797	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 45,896,379-50,762,357 , GRCh38 chr3: 45,879,883-50,749,922 , GRCh37 chr3: 45,921,375-50,787,353	RBM5-AS1, PRSS42P, 185 more genes
nsv984540	copy number variation	1	nstd91	human		NCBI36 chr3: 50,448,695-50,644,314 , GRCh37.p13 chr3: 50,473,691-50,669,310 , GRCh38.p12 chr3: 50,436,260-50,631,879	CISH, MAPKAPK3, 5 more genes
nsv429644	copy number variation	1	nstd11	human		GRCh37.p13 chr3: 35,009,045-84,383,151 , GRCh38.p12 chr3: 34,967,553-84,334,000 , NCBI36 chr3: 34,984,049-84,465,841	ACAA1, ACVR2B, 823 more genes
nsv6311797	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 50,431,520-50,685,477 , GRCh38.p12 chr3: 50,394,089-50,648,046	CACNA2D2, C3orf18, 6 more genes
nsv6311798	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 50,540,629-50,655,235 , GRCh38.p12 chr3: 50,503,198-50,617,804	MAPKAPK3, LOC105377083, 4 more genes
nsv3883874	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 50,435,928-50,732,729 , GRCh38.p12 chr3: 50,398,497-50,695,298	MIR4787, MAPKAPK3, 10 more genes
nsv984837	copy number variation	2	nstd11	human		GRCh37.p13 chr3: 60,345-197,896,118 , GRCh38.p12 chr3: 18,667-198,169,247 , NCBI36 chr3: 35,345-199,380,515	AADAC, ACAA1, 2982 more genes
nsv536567	copy number variation	1	nstd54	human		NCBI36 chr3: 50,458,041-50,654,595 , GRCh37.p13 chr3: 50,483,037-50,679,591 , GRCh38.p12 chr3: 50,445,606-50,642,160	C3orf18, HEMK1, 5 more genes
nsv6134694	copy number variation	1	nstd213	human		GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985	ACY1, AMT, 210 more genes
nsv6135016	copy number variation	1	nstd213	human		GRCh37 chr3: 48,760,000-52,290,001 , GRCh38.p12 chr3: 48,722,567-52,255,985	ACY1, ALAS1, 128 more genes
nsv2783669	copy number variation	1	nstd132	human		NCBI36 chr3: 50,266,789-50,667,176 , GRCh37.p13 chr3: 50,302,830-50,692,172 , GRCh38.p12 chr3: 50,254,353-50,654,741	GNAI2, MAPKAPK3, 23 more genes

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Organism

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Has Clinical Interpretation

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Items: 1 to 20 of 25

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Number of Variants: 20

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