b3gnt2[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
nsv3881797	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 62,412,202-62,533,045 , GRCh38.p12 chr2: 62,185,067-62,305,910	B3GNT2, LOC105374761, 2 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	B3GNT2, 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	B3GNT2, CYP1B1-AS1, 1649 more genes
nsv3892726	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 56,818,693-62,554,307 , GRCh38 chr2: 56,738,054-62,473,668 , GRCh37 chr2: 56,965,189-62,700,803	B3GNT2, RPS29P10, 66 more genes
nsv3903187	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 58,112,555-63,692,448 , GRCh38 chr2: 58,031,916-63,611,810 , GRCh37 chr2: 58,259,051-63,838,944	B3GNT2, RPL31P30, 76 more genes
nsv3904784	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 58,953,678-64,270,970 , GRCh37 chr2: 59,100,174-64,417,466 , GRCh38 chr2: 58,873,039-64,190,332	B3GNT2, UGP2, 79 more genes
nsv3902458	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 59,885,981-62,563,218 , NCBI36 chr2: 59,739,485-62,416,722 , GRCh38 chr2: 59,658,846-62,336,083	B3GNT2, MIR4432, 48 more genes
nsv3898402	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 61,596,077-62,386,487 , GRCh38 chr2: 61,515,438-62,305,848 , GRCh37 chr2: 61,742,573-62,532,983	B3GNT2, LOC100533678, 17 more genes
nsv997086	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr2: 58,912,065-62,261,736 , GRCh37 chr2: 59,139,200-62,488,871	B3GNT2, ATP1B3P1, 52 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	B3GNT2, 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	B3GNT2, 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	B3GNT2, 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	B3GNT2, MTND2P22, 3724 more genes
nsv3916821	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722	B3GNT2, NAGK, 595 more genes
nsv3900298	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 58,506,654-83,814,086 , GRCh38 chr2: 58,279,519-83,586,962 , NCBI36 chr2: 58,360,158-83,667,597	B3GNT2, MIR1285-2, 404 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	B3GNT2, ACTG2, 1713 more genes
nsv4347155	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 57,445,335-62,733,206 , GRCh38.p12 chr2: 57,218,200-62,506,071	B3GNT2, ATP1B3P1, 66 more genes
nsv3885478	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 61,701,437-65,731,084 , GRCh38.p12 chr2: 61,474,302-65,503,950	B3GNT2, MDH1, 80 more genes
nsv3872033	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr2: 61,372,285-62,496,451 , GRCh37.p13 chr2: 61,599,420-62,723,586	B3GNT2, XPO1, 23 more genes
nsv3870629	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr2: 62,302,506-62,602,053 , GRCh38.p12 chr2: 62,075,371-62,374,918	B3GNT2, LOC105374761, 5 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 26

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Number of Variants: 20

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Supplemental Content

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Search details

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