dbVar for Gene (Select 2248) - 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
nsv7143996	insertion	1	nstd232	human		GRCh37.p13 chr11: 69,628,592-69,628,592 , GRCh38.p12 chr11: 69,813,824-69,813,824	FGF3
nsv7094093	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473	B4GAT1, CHKA-DT, 208 more genes
nsv7075540	inversion	1	nstd229	human		GRCh38 chr11: 67,968,443-71,626,784 , GRCh37.p13 chr11: 67,735,914-71,337,830	S100A11P3, CCND1, 76 more genes
nsv6904338	copy number variation	1	nstd229	human		GRCh38 chr11: 69,155,401-69,991,100 , GRCh37.p13 chr11: 68,922,869-69,614,785	LOC338694, LOC105369370, 17 more genes
nsv6900732	copy number variation	1	nstd229	human		GRCh38 chr11: 69,588,671-70,124,332 , GRCh37.p13 chr11\|NW_003571046.1: 1-276,448 , GRCh37.p13 chr11: 69,403,439-69,970,438	FGF19, LOC105369371, 10 more genes
nsv6637600	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 69,559,588-70,347,818 , GRCh38.p12 chr11: 69,744,820-70,501,713	LOC107984368, ANO1, 15 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	PYGM, ATL3, 2125 more genes
nsv6290813	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 69,214,835-70,821,137 , GRCh38.p12 chr11: 69,400,067-71,110,091	CCND1, LOC101928473, 25 more genes
nsv6287312	insertion	1	nstd214	human		GRCh38 chr11: 69,813,824-69,813,824 , GRCh37.p13 chr11: 69,628,592-69,628,592 , GRCh37.p13 chr11\|NW_003571046.1: 13,807-13,807	FGF3
nsv6285807	insertion	1	nstd214	human		GRCh38 chr11: 69,813,816-69,813,816 , GRCh37.p13 chr11\|NW_003571046.1: 13,799-13,799 , GRCh37.p13 chr11: 69,628,584-69,628,584	FGF3
nsv6272993	copy number variation	1	nstd214	human		GRCh38 chr11: 69,813,654-69,813,717 , GRCh37.p13 chr11: 69,628,422-69,628,485 , GRCh37.p13 chr11\|NW_003571046.1: 13,637-13,700	FGF3
nsv6202326	copy number variation	1	nstd214	human		GRCh38 chr11: 69,813,712-69,813,767 , GRCh37.p13 chr11\|NW_003571046.1: 13,695-13,750 , GRCh37.p13 chr11: 69,628,480-69,628,535	FGF3
nsv6201705	copy number variation	1	nstd214	human		GRCh38 chr11: 69,813,648-69,813,751 , GRCh37.p13 chr11\|NW_003571046.1: 13,631-13,734 , GRCh37.p13 chr11: 69,628,416-69,628,519	FGF3
nsv6195446	copy number variation	1	nstd214	human		GRCh38 chr11: 69,813,560-69,813,759 , GRCh37.p13 chr11: 69,628,328-69,628,527 , GRCh37.p13 chr11\|NW_003571046.1: 13,543-13,742	FGF3
nsv6097676	insertion	1	nstd212	human		GRCh38 chr11: 69,813,775-69,813,775 , GRCh37.p13 chr11: 69,628,543-69,628,543 , GRCh37.p13 chr11\|NW_003571046.1: 13,758-13,758	FGF3
nsv6091599	insertion	1	nstd212	human		GRCh38 chr11: 69,813,638-69,813,638 , GRCh37.p13 chr11\|NW_003571046.1: 13,621-13,621 , GRCh37.p13 chr11: 69,628,406-69,628,406	FGF3
nsv6022118	copy number variation	1	nstd212	human		GRCh38 chr11: 69,813,701-69,813,816 , GRCh37.p13 chr11\|NW_003571046.1: 13,684-13,799 , GRCh37.p13 chr11: 69,628,469-69,628,584	FGF3
nsv5658107	insertion	1	nstd207	human		GRCh38 chr11: 69,813,600-69,813,600 , GRCh37.p13 chr11\|NW_003571046.1: 13,583-13,583 , GRCh37.p13 chr11: 69,628,368-69,628,368	FGF3
nsv5584748	copy number variation	1	nstd207	human		GRCh38 chr11: 69,813,576-69,813,647 , GRCh37.p13 chr11\|NW_003571046.1: 13,559-13,630 , GRCh37.p13 chr11: 69,628,344-69,628,415	FGF3
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

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Number of Variants: 20

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Organism

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Sex of Subject

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Items: 1 to 20 of 113

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Number of Variants: 20

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