dbVar for Gene (Select 6591) - 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
nsv5482885	copy number variation	1	nstd206	human		GRCh38 chr8: 48,917,593-48,917,743 , GRCh37.p13 chr8: 49,830,152-49,830,302	SNAI2
nsv5477355	copy number variation	1	nstd206	human		GRCh38 chr8: 48,911,830-48,917,369 , GRCh37.p13 chr8: 49,824,389-49,829,928	SNAI2
nsv5115110	mobile element insertion	1	nstd203	human		GRCh38 chr8: 48,921,069-48,921,086 , GRCh37.p13 chr8: 49,833,628-49,833,645	LOC107986942, SNAI2
nsv4965252	copy number variation	1	nstd200	human		GRCh38 chr8: 48,860,856-48,997,271 , GRCh37.p13 chr8: 49,773,415-49,909,830	SNAI2, LOC107986942
nsv4952153	copy number variation	1	nstd200	human		GRCh38 chr8: 48,911,829-48,917,369 , GRCh37.p13 chr8: 49,824,388-49,829,928	SNAI2
nsv4812984	copy number variation	1	nstd200	human		GRCh37 chr8: 49,830,152-49,830,302 , GRCh38.p12 chr8: 48,917,593-48,917,743	SNAI2
nsv4812983	copy number variation	1	nstd200	human		GRCh37 chr8: 49,824,388-49,829,928 , GRCh38.p12 chr8: 48,911,829-48,917,369	SNAI2
nsv4768211	inversion	1	nstd199	human		GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538	, ADRA1A, 411 more genes
nsv4756879	inversion	1	nstd199	human		GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373	, ADRA1A, 411 more genes
nsv4715498	copy number variation	1	nstd195	human		GRCh37 chr8: 49,712,451-49,851,651 , GRCh38.p12 chr8: 48,799,892-48,939,092	SNAI2, LOC105375825, 1 more genes
nsv4709673	copy number variation	1	nstd195	human		GRCh37 chr8: 49,712,301-49,851,601 , GRCh38.p12 chr8: 48,799,742-48,939,042	SNAI2, LOC105375825, 1 more genes
nsv4543321	insertion	1	nstd166	human		GRCh37.p13 chr8: 49,830,369-49,830,369 , GRCh38.p12 chr8: 48,917,810-48,917,810	SNAI2
nsv4456871	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530	CRIPTOP5, TRIM60P15, 297 more genes
nsv4456811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385	TERF1, LOC107986945, 1511 more genes
nsv4452294	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 48,270,390-49,987,806 , GRCh38.p12 chr8: 47,357,823-49,075,247	LOC100420532, LOC107986941, 29 more genes
nsv4349554	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385	LOC101929488, TEX15, 2105 more genes
nsv4172428	copy number variation	1	nstd166	human		GRCh37.p13 chr8: 49,830,152-49,830,302 , GRCh38.p12 chr8: 48,917,593-48,917,743	SNAI2
nsv4170904	copy number variation	1	nstd166	human		GRCh37.p13 chr8: 49,620,939-50,612,109 , GRCh38.p12 chr8: 48,708,380-49,699,549	SNAI2, CLXN, 7 more genes
nsv4168728	copy number variation	1	nstd166	human		GRCh37.p13 chr8: 49,824,389-49,829,928 , GRCh38.p12 chr8: 48,911,830-48,917,369	SNAI2
nsv3963430	copy number variation	1	nstd168	human		GRCh38 chr8: 48,897,266-48,943,558 , GRCh37.p13 chr8: 49,809,825-49,856,117	LOC107986942, SNAI2

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Items: 1 to 20 of 111

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Number of Variants: 20

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