b3gnt4[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
nsv4455138	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 122,681,331-122,730,394 , GRCh38.p12 chr12: 122,196,784-122,245,847	B3GNT4, LRRC43, 3 more genes
nsv3903823	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 122,676,019-122,710,016 , GRCh38.p12 chr12: 122,191,472-122,225,469	B3GNT4, LOC101593348, 2 more genes
nsv4455692	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 122,169,403-129,084,163 , GRCh38.p12 chr12: 121,731,497-128,599,618	B3GNT4, LOC107987176, 147 more genes
nsv3923612	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 120,718,786-127,500,215 , GRCh37 chr12: 121,156,589-127,984,760 , NCBI36 chr12: 119,640,972-126,550,713	B3GNT4, NCOR2, 161 more genes
nsv3916210	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 122,355,664-128,287,262 , GRCh38 chr12: 121,917,758-127,802,717 , NCBI36 chr12: 120,840,047-126,853,215	B3GNT4, RILPL2, 129 more genes
nsv3921651	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 119,426,254-121,510,218 , GRCh37 chr12: 120,941,871-122,944,265 , GRCh38 chr12: 120,504,068-122,459,718	B3GNT4, ACADS, 58 more genes
nsv3922210	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 120,248,060-121,556,029 , GRCh37 chr12: 121,956,483-122,990,076 , GRCh38 chr12: 121,325,874-122,505,529	B3GNT4, KDM2B-DT, 31 more genes
nsv3915645	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 120,393,186-121,510,218 , GRCh38 chr12: 121,471,000-122,459,718 , GRCh37 chr12: 121,956,483-122,944,265	B3GNT4, IL31, 26 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	B3GNT4, RNA5SP369, 2454 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	B3GNT4, LOH12CR2, 2452 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	B3GNT4, RNU4ATAC16P, 2452 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	B3GNT4, BTG1P1, 2451 more genes
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	B3GNT4, OR5BT1P, 2441 more genes
nsv3913894	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 113,190,591-132,287,975 , GRCh38 chr12: 114,268,403-133,201,316 , GRCh37 chr12: 114,706,208-133,777,902	B3GNT4, TAOK3, 386 more genes
nsv3924220	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 115,131,583-133,166,920 , NCBI36 chr12: 114,053,771-132,253,579 , GRCh37 chr12: 115,569,388-133,743,506	B3GNT4, LOC105370080, 376 more genes
nsv3920557	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 118,603,264-133,758,908 , GRCh38 chr12: 118,165,459-133,182,322 , NCBI36 chr12: 117,087,647-132,268,981	B3GNT4, TMED2, 339 more genes
nsv3896575	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 120,367,241-133,777,645 , GRCh38.p12 chr12: 119,929,437-133,201,059	B3GNT4, LOC107984448, 306 more genes
nsv3923347	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 119,619,858-132,289,149 , GRCh37 chr12: 121,135,475-133,779,076 , GRCh38 chr12: 120,697,672-133,202,490	B3GNT4, LOC105370044, 273 more genes
nsv6290239	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809	B3GNT4, ACADS, 356 more genes
nsv7094203	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 122,277,634-124,242,579 , GRCh38.p12 chr12: 121,839,728-123,758,032	B3GNT4, SBNO1, 58 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 27

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Number of Variants: 20

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Supplemental Content

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