sult1c3[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
nsv3882761	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 108,852,039-108,856,175 , GRCh38.p12 chr2: 108,235,583-108,239,719	SULT1C3
nsv3873220	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 108,855,168-108,856,175 , GRCh38.p12 chr2: 108,238,712-108,239,719	SULT1C3
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	SULT1C3, DAZAP2P1, 2991 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	SULT1C3, CYP1B1-AS1, 1649 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	SULT1C3, SMIM12P1, 189 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	SULT1C3, RPL10P5, 121 more genes
nsv6313505	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 108,446,955-110,504,318 , GRCh38.p12 chr2: 107,830,499-109,746,741	SULT1C3, SH3RF3-AS1, 37 more genes
nsv7095847	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr2: 108,604,612-109,579,739 , GRCh38.p12 chr2: 107,988,156-108,963,283	SULT1C3, ACTP1, 21 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	SULT1C3, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	SULT1C3, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	SULT1C3, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	SULT1C3, MTND2P22, 3724 more genes
nsv3876227	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 96,353,030-114,045,463 , GRCh38.p12 chr2: 95,687,282-113,287,886	SULT1C3, RNU4-8P, 346 more genes
nsv3902899	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 94,707,984-111,076,455 , GRCh38 chr2: 94,678,532-110,602,409 , GRCh37 chr2: 95,344,257-111,359,986	SULT1C3, MTCO3P45, 325 more genes
nsv3907326	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 97,672,522-110,211,318 , GRCh37 chr2: 98,288,985-110,968,895 , NCBI36 chr2: 97,655,417-110,326,184	SULT1C3, RPL22P11, 212 more genes
nsv3894687	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 102,327,287-111,548,995 , GRCh38 chr2: 101,710,825-110,791,418 , NCBI36 chr2: 101,693,719-111,265,466	SULT1C3, NCK2, 162 more genes
nsv3906499	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 100,361,404-108,455,759 , GRCh37 chr2: 100,994,972-109,089,327 , GRCh38 chr2: 100,378,510-108,472,871	SULT1C3, LOC105373511, 132 more genes
nsv6314726	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196	SULT1C3, ACTG2, 1713 more genes
nsv3881702	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 107,020,782-111,365,996 , GRCh38.p12 chr2: 106,404,326-110,608,419	SULT1C3, CD8B2, 87 more genes
nsv6290767	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 107,020,782-110,068,385 , GRCh38.p12 chr2: 106,404,326-109,451,929	SULT1C3, CD8B2, 43 more genes

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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 41

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Number of Variants: 20

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Supplemental Content

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