dbVar for Gene (Select 10984) - 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
nsv7137183	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 2,683,186-2,683,314 , GRCh38.p12 chr11: 2,661,956-2,662,084	KCNQ1OT1, KCNQ1
nsv7094186	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 721,044-3,988,932 , GRCh38.p12 chr11: 721,044-3,967,702	OR7E117P, RPLP2, 124 more genes
nsv7094163	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 2,549,148-2,683,321 , GRCh38.p12 chr11: 2,527,918-2,662,091	KCNQ1OT1, KCNQ1
nsv7093846	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 2,629,548-2,721,238 , GRCh38.p12 chr11: 2,608,318-2,700,008	KCNQ1, KCNQ1OT1
nsv7093845	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 2,466,329-2,869,233 , GRCh38.p12 chr11: 2,445,099-2,848,003	COX6CP18, KCNQ1, 2 more genes
nsv7093761	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 1,278,740-2,906,719 , GRCh38.p12 chr11: 1,257,510-2,885,489	TOLLIP-DT, KRTAP5-6, 58 more genes
nsv7072778	inversion	1	nstd229	human		GRCh38 chr11: 2,602,398-2,613,291 , GRCh37.p13 chr11: 2,623,628-2,634,521	KCNQ1OT1, KCNQ1
nsv6917856	copy number variation	1	nstd229	human		GRCh38 chr11: 2,676,689-2,679,666 , GRCh37.p13 chr11: 2,697,919-2,700,896	KCNQ1, KCNQ1OT1
nsv6917303	copy number variation	1	nstd229	human		GRCh38 chr11: 2,669,525-2,671,124 , GRCh37.p13 chr11: 2,690,755-2,692,354	KCNQ1, KCNQ1OT1
nsv6917011	copy number variation	1	nstd229	human		GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062	LOC105376526, OR51E2, 279 more genes
nsv6915487	copy number variation	1	nstd229	human		GRCh38 chr11: 2,684,601-2,736,300 , GRCh37.p13 chr11: 2,705,831-2,757,530	KCNQ1, KCNQ1OT1
nsv6911875	copy number variation	1	nstd229	human		GRCh38 chr11: 2,667,891-2,671,037 , GRCh37.p13 chr11: 2,689,121-2,692,267	KCNQ1, KCNQ1OT1
nsv6909713	copy number variation	1	nstd229	human		GRCh38 chr11: 2,672,078-2,675,085 , GRCh37.p13 chr11: 2,693,308-2,696,315	KCNQ1, KCNQ1OT1
nsv6909220	copy number variation	1	nstd229	human		GRCh38 chr11: 2,673,782-2,673,884 , GRCh37.p13 chr11: 2,695,012-2,695,114	KCNQ1OT1, KCNQ1
nsv6905139	copy number variation	1	nstd229	human		GRCh38 chr11: 2,624,048-2,629,375 , GRCh37.p13 chr11: 2,645,278-2,650,605	KCNQ1OT1, KCNQ1
nsv6904115	copy number variation	1	nstd229	human		GRCh38 chr11: 2,691,001-2,693,300 , GRCh37.p13 chr11: 2,712,231-2,714,530	KCNQ1OT1, KCNQ1
nsv6901914	copy number variation	1	nstd229	human		GRCh38 chr11: 2,592,479-2,621,406 , GRCh37.p13 chr11: 2,613,709-2,642,636	KCNQ1, KCNQ1OT1
nsv6901626	copy number variation	1	nstd229	human		GRCh38 chr11: 2,601,096-2,606,666 , GRCh37.p13 chr11: 2,622,326-2,627,896	KCNQ1, KCNQ1OT1
nsv6885276	copy number variation	1	nstd229	human		GRCh38 chr11: 1,136,035-3,145,463 , GRCh37.p13 chr11: 1,129,943-3,166,693	KRTAP5-1, MIR675, 69 more genes
nsv6637864	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177	PNPLA2, OR52H1, 372 more genes

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Items: 1 to 20 of 270

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Number of Variants: 20

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