dbVar for Gene (Select 4793) - 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
nsv7095479	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 38,375,572-39,738,787 , GRCh38.p12 chr19: 37,884,932-39,248,147	HNRNPL, RN7SL663P, 45 more genes
nsv7095205	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr19: 39,205,089-40,913,839 , GRCh38.p12 chr19: 38,714,449-40,407,932	CCNP, NFKBIB, 81 more genes
nsv7064872	inversion	1	nstd229	human		GRCh38 chr19: 38,901,471-38,917,132 , GRCh37.p13 chr19: 39,392,111-39,407,772	CCER2, NFKBIB, 1 more genes
nsv7018029	copy number variation	1	nstd229	human		GRCh38 chr19: 38,899,495-38,899,689 , GRCh37.p13 chr19: 39,390,135-39,390,329	SIRT2, NFKBIB
nsv7008156	copy number variation	1	nstd229	human		GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048	LOC105372390, LOC107985291, 396 more genes
nsv7005713	copy number variation	1	nstd229	human		GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386	, TYROBP, 259 more genes
nsv7002869	copy number variation	1	nstd229	human		GRCh38 chr19: 38,872,385-39,331,882 , GRCh37.p13 chr19: 39,363,025-39,822,522	IFNL4P1, IFNL4, 19 more genes
nsv6998425	copy number variation	1	nstd229	human		GRCh38 chr19: 38,900,571-38,930,432 , GRCh37.p13 chr19: 39,391,211-39,421,072	NFKBIB, CCER2, 2 more genes
nsv6597106	inversion	1	nstd223	human		GRCh38 chr19: 38,901,945-38,903,045 , GRCh37.p13 chr19: 39,392,585-39,393,685	NFKBIB
nsv6531882	copy number variation	1	nstd223	human		GRCh38 chr19: 38,872,385-39,331,882 , GRCh37.p13 chr19: 39,363,025-39,822,522	NFKBIB, IFNL3, 19 more genes
nsv6524996	copy number variation	1	nstd223	human		GRCh38 chr19: 38,897,789-38,898,814 , GRCh37.p13 chr19: 39,388,429-39,389,454	NFKBIB, SIRT2
nsv6290300	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324	ZNF420, LOC105372330, 574 more genes
nsv6281395	copy number variation	1	nstd214	human		GRCh38 chr19: 38,902,484-38,902,565 , GRCh37.p13 chr19: 39,393,124-39,393,205	NFKBIB
nsv6145831	copy number variation	1	nstd206	human		GRCh38 chr19: 38,896,874-38,904,874 , GRCh37.p13 chr19: 39,387,514-39,395,514	SIRT2, NFKBIB
nsv6145796	copy number variation	1	nstd206	human		GRCh38 chr19: 38,904,874-38,912,874 , GRCh37.p13 chr19: 39,395,514-39,403,514	CCER2, NFKBIB
nsv6144358	copy number variation	1	nstd206	human		GRCh38 chr19: 38,852,874-38,930,874 , GRCh37.p13 chr19: 39,343,514-39,421,514	NFKBIB, MRPS12, 4 more genes
nsv6133523	copy number variation	1	nstd213	human		GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083	, ACTN4, 345 more genes
nsv6042282	copy number variation	1	nstd212	human		GRCh38 chr19: 38,902,505-38,902,584 , GRCh37.p13 chr19: 39,393,145-39,393,224	NFKBIB
nsv5977088	insertion	1	nstd209	human		GRCh38 chr19: 38,902,085-38,902,085 , GRCh37.p13 chr19: 39,392,725-39,392,725	NFKBIB
nsv5596919	copy number variation	1	nstd207	human		GRCh38 chr19: 38,902,484-38,902,565 , GRCh37.p13 chr19: 39,393,124-39,393,205	NFKBIB

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Number of Variants: 20

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 197

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Number of Variants: 20

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