dbVar for Gene (Select 55539) - 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
nsv5918738	copy number variation	1	nstd209	human		GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188	, TALDO1, 128 more genes
nsv5498408	copy number variation	1	nstd206	human		GRCh38 chr11: 2,872,300-2,873,583 , GRCh37.p13 chr11: 2,893,530-2,894,813	KCNQ1DN
nsv5380885	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798	LINC02688, MIR210, 156 more genes
nsv5305191	copy number variation	1	nstd204	human		GRCh38.p13 chr11: 2,868,772-2,869,108 , GRCh37.p13 chr11: 2,890,002-2,890,338	KCNQ1DN
nsv4768373	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811	LOC107984302, STK33, 375 more genes
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
nsv4729112	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307	OR51E1, TNNI2, 203 more genes
nsv4728919	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 2,629,917-2,902,668 , GRCh38.p12 chr11: 2,608,687-2,881,438	KCNQ1-AS1, KCNQ1, 4 more genes
nsv4681827	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 532,616-2,906,985 , GRCh38.p12 chr11: 532,616-2,885,755	LOC105376517, KRTAP5-2, 99 more genes
nsv4679705	copy number variation	1	nstd189	human		GRCh37.p13 chr11: 2,339,823-3,832,257 , GRCh38.p12 chr11: 2,318,593-3,811,027	, ART1, 50 more genes
nsv4675579	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 2,683,937-3,207,439 , GRCh38.p12 chr11\|NT_187585.1: 1-296,883 , GRCh38.p12 chr11: 2,662,707-3,186,209	CDKN1C, KCNQ1DN, 15 more genes
nsv4674879	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449	BGLT3, RPL21P97, 723 more genes
nsv4350476	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589	KRTAP5-3, OR56A7P, 457 more genes
nsv4195249	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 2,893,577-2,894,764 , GRCh38.p12 chr11\|NT_187585.1: 104,520-105,707 , GRCh38.p12 chr11: 2,872,347-2,873,534	KCNQ1DN
nsv3924864	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 1,996,741-3,645,369 , NCBI36 chr11: 1,953,317-3,601,945 , GRCh38 chr11: 1,975,511-3,624,139	TSSC2, CD81, 54 more genes
nsv3922910	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 1,116,807-3,191,729 , GRCh38 chr11: 1,132,899-3,213,923 , GRCh37 chr11: 1,126,807-3,235,153	CARS1-AS1, TH, 69 more genes
nsv3919565	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092	OR51A7, OR51F5P, 437 more genes
nsv3919461	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 1,515,185-3,338,575 , GRCh38 chr11: 1,537,379-3,360,769 , GRCh37 chr11: 1,558,609-3,381,999	C11orf21, SLC22A18AS, 67 more genes
nsv3918376	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 128,203-5,440,733 , GRCh37.p13 chr11: 138,203-5,484,157 , GRCh38.p12 chr11: 138,203-5,462,927	HBG2, OR51T1, 262 more genes
nsv3916105	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 186,966-4,413,150 , GRCh38 chr11: 196,966-4,435,344 , GRCh37 chr11: 196,966-4,456,574	MRPL23, CRACR2B, 181 more genes

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Has Clinical Interpretation

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Items: 1 to 20 of 156

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Number of Variants: 20

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