zc3h6[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
nsv3876315	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 113,045,654-113,047,747 , GRCh38.p12 chr2: 112,288,077-112,290,170	ZC3H6
nsv3886755	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 113,041,461-113,091,685 , GRCh38.p12 chr2: 112,283,884-112,334,108	ZC3H6, NDUFB4P6
nsv3882002	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 113,042,446-113,082,151 , GRCh38.p12 chr2: 112,284,869-112,324,574	ZC3H6, NDUFB4P6
nsv3889355	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 113,041,461-113,063,714 , GRCh38.p12 chr2: 112,283,884-112,306,137	ZC3H6, NDUFB4P6
nsv3874969	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 113,041,461-113,053,061 , GRCh38.p12 chr2: 112,283,884-112,295,484	ZC3H6, NDUFB4P6
nsv3880871	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 113,041,461-113,048,705 , GRCh38.p12 chr2: 112,283,884-112,291,128	ZC3H6, NDUFB4P6
nsv3886703	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 113,042,446-113,048,705 , GRCh38.p12 chr2: 112,284,869-112,291,128	ZC3H6, NDUFB4P6
nsv6314501	complex chromosomal rearrangement	2	nstd102	human	Uncertain significance	GRCh38.p12 chr2: 87,966,166-87,966,166 , GRCh38.p12 chr2: 87,972,613-87,972,613 , GRCh38.p12 chr2: 112,288,667-112,288,667 , GRCh38.p12 chr2: 112,291,103-112,291,103 , GRCh37 chr2: 88,265,685-88,265,685 , GRCh37 chr2: 88,272,132-88,272,132 , GRCh37 chr2: 113,046,244-113,046,244 , GRCh37 chr2: 113,048,680-113,048,680	ZC3H6, RGPD2, 1 more genes
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	ZC3H6, DAZAP2P1, 2991 more genes
nsv3873957	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 109,798,247-125,658,380 , GRCh38.p12 chr2: 109,181,791-124,900,803	ZC3H6, MTND1P28, 230 more genes
nsv3872550	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 106,423,310-115,054,828 , GRCh38.p12 chr2: 105,806,853-114,297,251	ZC3H6, SMIM12P1, 189 more genes
nsv3888610	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 109,556,627-117,570,152 , GRCh38.p12 chr2: 108,940,171-116,812,576	ZC3H6, LOC112268438, 149 more genes
nsv4728410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 107,029,680-113,187,742 , GRCh38.p12 chr2: 106,413,224-112,430,165	ZC3H6, RPL10P5, 121 more genes
nsv3876697	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 110,980,294-113,137,529 , GRCh38.p12 chr2: 110,222,717-112,379,952	ZC3H6, ANAPC1, 47 more genes
nsv7148080	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 111,335,152-113,127,204 , GRCh38.p12 chr2: 110,577,575-112,369,627	ZC3H6, MIR4771-2, 33 more genes
nsv6636225	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 111,369,264-113,142,794 , GRCh38.p12 chr2: 110,611,687-112,385,217	ZC3H6, RPL34P8, 32 more genes
nsv6636824	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 111,366,256-113,127,751 , GRCh38.p12 chr2: 110,608,679-112,370,174	ZC3H6, PAFAH1B1P2, 33 more genes
nsv3883679	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 111,366,255-113,111,856 , GRCh38.p12 chr2: 110,608,678-112,354,279	ZC3H6, RTRAFP1, 32 more genes
nsv4347217	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 111,395,351-113,102,594 , GRCh38.p12 chr2: 110,637,774-112,345,017	ZC3H6, LOC101927283, 29 more genes
nsv1398125	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 111,398,336-113,101,220 , GRCh38.p12 chr2: 110,640,759-112,343,643	ZC3H6, ACOXL-AS1, 28 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 68

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Number of Variants: 20

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