dbVar for Gene (Select 29125) - 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
nsv5604483	copy number variation	1	nstd207	human		GRCh38 chr11: 2,300,166-2,300,224 , GRCh37.p13 chr11: 2,321,396-2,321,454	C11orf21, TSPAN32
nsv5510547	copy number variation	1	nstd206	human		GRCh38 chr11: 2,296,264-2,296,319 , GRCh37.p13 chr11: 2,317,494-2,317,549	C11orf21
nsv5502684	copy number variation	1	nstd206	human		GRCh38 chr11: 2,300,085-2,330,106 , GRCh37.p13 chr11: 2,321,315-2,351,336	CD81-AS1, TSPAN32, 2 more genes
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
nsv5248411	copy number variation	1	nstd204	human		GRCh38.p13 chr11: 2,298,001-2,305,800 , GRCh37.p13 chr11: 2,319,231-2,327,030	TSPAN32, C11orf21
nsv4984138	copy number variation	1	nstd200	human		GRCh38 chr11: 2,300,061-2,330,106 , GRCh37.p13 chr11: 2,321,291-2,351,336	RNU6-878P, CD81-AS1, 2 more genes
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
nsv4735849	copy number variation	1	nstd199	human		GRCh37 chr11: 2,321,309-2,321,387 , GRCh38.p12 chr11: 2,300,079-2,300,157	TSPAN32, C11orf21
nsv4729545	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 1,436,158-2,321,134 , GRCh38.p12 chr11: 1,414,928-2,299,904	MIR4686, H19, 40 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
nsv4728784	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 2,316,896-2,418,571 , GRCh38.p12 chr11: 2,295,666-2,397,341	LOC105376520, CD81, 6 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
nsv4675807	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 2,209,396-2,520,511 , GRCh38.p12 chr11: 2,188,166-2,499,281	ASCL2, CD81, 9 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
nsv4606352	copy number variation	1	nstd183	human		GRCh37 chr11: 2,320,897-2,321,557 , GRCh38.p12 chr11: 2,299,667-2,300,327	C11orf21, TSPAN32
nsv4606254	copy number variation	1	nstd183	human		GRCh37 chr11: 2,320,812-2,321,557 , GRCh38.p12 chr11: 2,299,582-2,300,327	TSPAN32, C11orf21
nsv4528738	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 2,317,494-2,317,549 , GRCh38.p12 chr11: 2,296,264-2,296,319	C11orf21
nsv4485698	mobile element insertion	1	nstd166	human		GRCh37.p13 chr11: 2,319,567-2,319,567 , GRCh38.p12 chr11: 2,298,337-2,298,337	TSPAN32, C11orf21

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Number of Variants: 20

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