b4galnt4[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
nsv3900324	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 353,376-428,582 , GRCh38.p12 chr11: 353,376-428,582	B4GALNT4, SIGIRR, 2 more genes
nsv3894333	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 356,090-428,582 , GRCh38.p12 chr11: 356,090-428,582	B4GALNT4, ANO9, 2 more genes
nsv3908470	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 368,778-428,582 , GRCh38.p12 chr11: 368,778-428,582	B4GALNT4, SIGIRR, 2 more genes
nsv3922604	copy number variation	1	nstd102	human	Benign	NCBI36 chr11: 349,217-404,570 , GRCh38 chr11: 359,217-414,570 , GRCh37 chr11: 359,217-414,570	B4GALNT4, PKP3, 1 more genes
nsv3915428	copy number variation	1	nstd102	human	Benign	GRCh38 chr11: 371,634-426,161 , GRCh37 chr11: 371,634-426,161 , NCBI36 chr11: 361,634-416,161	B4GALNT4, ANO9, 2 more genes
nsv3899227	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 377,278-428,582 , GRCh38.p12 chr11: 377,278-428,582	B4GALNT4, SIGIRR, 2 more genes
nsv3918899	copy number variation	1	nstd102	human	Benign/Likely benign	NCBI36 chr11: 361,634-404,570 , GRCh38 chr11: 371,634-414,570 , GRCh37 chr11: 371,634-414,570	B4GALNT4, PKP3, 1 more genes
nsv3892826	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 368,778-408,352 , GRCh38.p12 chr11: 368,778-408,352	B4GALNT4, SIGIRR, 1 more genes
nsv7137204	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 268,586-748,873 , GRCh38.p12 chr11: 268,586-748,873	B4GALNT4, PKP3, 32 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	B4GALNT4, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	B4GALNT4, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	B4GALNT4, IGHMBP2, 2829 more genes
nsv3898926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-37,698,540 , GRCh38.p12 chr11: 230,615-37,676,990	B4GALNT4, OR51L1, 771 more genes
nsv4674879	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449	B4GALNT4, BGLT3, 723 more genes
nsv3906221	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673	B4GALNT4, PCNAP4, 688 more genes
nsv6315535	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599	B4GALNT4, OR52Q1P, 630 more genes
nsv3894525	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-25,584,362 , GRCh38.p12 chr11: 230,615-25,562,816	B4GALNT4, SDHCP4, 620 more genes
nsv3898948	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-17,099,213 , GRCh38.p12 chr11: 230,615-17,077,666	B4GALNT4, MTND5P21, 506 more genes
nsv4350476	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589	B4GALNT4, KRTAP5-3, 457 more genes
nsv3919565	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092	B4GALNT4, OR51A7, 437 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 47

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Number of Variants: 20

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