dbVar for Gene (Select 595) - 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
nsv5509951	copy number variation	1	nstd206	human		GRCh38 chr11: 69,648,886-69,648,952 , GRCh37.p13 chr11: 69,463,654-69,463,720	CCND1
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	FAUP4, MMP7, 2031 more genes
nsv5345065	translocation	1	nstd200	human		GRCh37 chr11: 69,463,654-69,463,654 , GRCh37 chr11: 69,463,720-69,463,720 , GRCh38.p12 chr11: 69,648,886-69,648,886 , GRCh38.p12 chr11: 69,648,952-69,648,952	CCND1
nsv4751865	inversion	1	nstd199	human		GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187	, ACP2, 1686 more genes
nsv4710825	copy number variation	1	nstd195	human		GRCh37 chr11: 69,409,751-69,724,701 , GRCh38.p12 chr11: 69,594,983-69,909,959	CCND1, FGF3, 5 more genes
nsv4706518	copy number variation	1	nstd195	human		GRCh37 chr11: 69,139,801-69,724,701 , GRCh38.p12 chr11: 69,325,035-69,909,959	FGF3, LOC107984368, 9 more genes
nsv4672846	copy number variation	1	nstd186	human		GRCh37 chr11: 69,454,101-69,458,500 , GRCh38.p12 chr11: 69,639,333-69,643,732	CCND1
nsv4614731	copy number variation	1	nstd183	human		GRCh37 chr11: 69,454,101-69,458,500 , GRCh38.p12 chr11: 69,639,333-69,643,732	CCND1
nsv4372377	copy number variation	1	nstd173	human		GRCh37 chr11: 69,451,837-69,472,571 , GRCh38.p12 chr11: 69,637,069-69,657,803	CCND1
nsv4210110	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 69,460,966-69,461,056 , GRCh38.p12 chr11: 69,646,198-69,646,288	CCND1
nsv3917463	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr11: 67,555,736-70,982,189 , GRCh37 chr11: 67,799,160-71,304,541 , GRCh38 chr11: 68,031,693-71,593,495	CCND1, CHKA, 71 more genes
nsv3909768	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 67,799,160-70,701,268 , GRCh38.p12 chr11: 68,031,693-70,855,163	CCND1, CHKA, 56 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	IGHMBP2, SYTL2, 2829 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	RTN3, KRTAP5-13P, 2833 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	LOC105376598, OSBPL9P2, 2842 more genes
nsv3156693	copy number variation	11	nstd151	human		GRCh37 chr11: 69,458,597-69,458,959 , GRCh38.p12 chr11: 69,643,829-69,644,191	CCND1
nsv3154722	copy number variation	1	nstd151	human		GRCh37 chr11: 69,458,597-70,507,877 , GRCh38.p12 chr11: 69,643,829-70,661,772	, LTO1, 22 more genes
nsv3144538	copy number variation	1	nstd151	human		GRCh37 chr11: 69,063,056-70,338,575 , GRCh38.p12 chr11: 69,295,589-70,492,470	, FADD, 27 more genes
esv3977039	copy number variation	3	estd229	human		GRCh37 chr11: 69,452,358-69,464,897 , GRCh38.p12 chr11: 69,637,590-69,650,129	CCND1
esv3977040	copy number variation	1	estd229	human		GRCh37 chr11: 69,452,358-69,464,897 , GRCh38.p12 chr11: 69,637,590-69,650,129	CCND1

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Items: 1 to 20 of 109

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Number of Variants: 20

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