dbVar for Gene (Select 84340) - 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
nsv6127597	insertion	1	nstd186	human		GRCh37 chr5: 74,055,092-74,055,127 , GRCh38.p12 chr5: 74,759,267-74,759,302	GFM2
nsv5843416	copy number variation	1	nstd209	human		GRCh38 chr5: 74,758,193-74,760,336 , GRCh37.p13 chr5: 74,054,018-74,056,161	GFM2
nsv5720955	mobile element insertion	1	nstd211	human		GRCh38 chr5: 74,754,406-74,754,406 , GRCh37.p13 chr5: 74,050,231-74,050,231	GFM2
nsv5673764	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 73,981,066-74,017,020 , GRCh38.p12 chr5: 74,685,241-74,721,195	HEXB, GFM2
nsv5629465	insertion	1	nstd207	human		GRCh38 chr5: 74,759,251-74,759,251 , GRCh37.p13 chr5: 74,055,076-74,055,076	GFM2
nsv5560947	sequence alteration	1	nstd206	human		GRCh38 chr5: 74,581,386-75,393,871 , GRCh37.p13 chr5: 73,877,211-74,689,696	HEXB, GFM2, 18 more genes
nsv5555957	mobile element insertion	1	nstd206	human		GRCh38 chr5: 74,754,422-74,754,457 , GRCh37.p13 chr5: 74,050,247-74,050,282	GFM2
nsv5543079	insertion	1	nstd206	human		GRCh38 chr5: 74,759,267-74,759,302 , GRCh37.p13 chr5: 74,055,092-74,055,127	GFM2
nsv5464128	copy number variation	1	nstd206	human		GRCh38 chr5: 74,722,204-74,722,271 , GRCh37.p13 chr5: 74,018,029-74,018,096	GFM2
nsv5461165	copy number variation	1	nstd206	human		GRCh38 chr5: 74,721,390-74,721,593 , GRCh37.p13 chr5: 74,017,215-74,017,418	HEXB, GFM2
nsv5096608	mobile element insertion	1	nstd203	human		GRCh38 chr5: 74,759,251-74,759,267 , GRCh37.p13 chr5: 74,055,076-74,055,092	GFM2
nsv5084422	mobile element insertion	1	nstd203	human		GRCh38 chr5: 74,759,256-74,759,267 , GRCh37.p13 chr5: 74,055,081-74,055,092	GFM2
nsv4725707	insertion	1	nstd186	human		GRCh37 chr5: 74,055,076-74,055,076 , GRCh38.p12 chr5: 74,759,251-74,759,251	GFM2
nsv4675667	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166	LOC101929380, LIX1-AS1, 318 more genes
nsv4675088	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 72,829,994-74,076,751 , GRCh38.p12 chr5: 73,534,169-74,780,926	NSA2, RNU7-196P, 17 more genes
nsv4567999	mobile element insertion	1	nstd166	human		GRCh37.p13 chr5: 74,018,823-74,018,823 , GRCh38.p12 chr5: 74,722,998-74,722,998	GFM2
nsv4566858	mobile element insertion	1	nstd166	human		GRCh37.p13 chr5: 74,035,748-74,035,748 , GRCh38.p12 chr5: 74,739,923-74,739,923	GFM2
nsv4553405	insertion	1	nstd166	human		GRCh37.p13 chr5: 74,055,076-74,055,076 , GRCh38.p12 chr5: 74,759,251-74,759,251	GFM2
nsv4436202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379	RNU1-150P, RNU6-727P, 1757 more genes
nsv4129204	copy number variation	1	nstd166	human		GRCh37.p13 chr5: 73,993,573-74,074,974 , GRCh38.p12 chr5: 74,697,748-74,779,149	HEXB, NSA2, 4 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

Links from Gene

Items: 1 to 20 of 138

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Number of Variants: 20

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