dbVar for Gene (Select 728192) - 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
nsv7148239	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 98,343,655-110,990,677 , GRCh37.p13 chr13: 98,995,909-111,643,024	CLYBL-AS3, PPIAP24, 162 more genes
nsv6955288	copy number variation	1	nstd229	human		GRCh38 chr13: 106,045,375-107,281,617 , GRCh37.p13 chr13: 106,697,724-107,933,965	LINC00443, NALF1, 13 more genes
nsv6953819	copy number variation	1	nstd229	human		GRCh38 chr13: 106,358,817-106,431,464 , GRCh37.p13 chr13: 107,011,165-107,083,812	RPL35P9, LOC107984626, 2 more genes
nsv6638047	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258	CUL4A, LOC105370373, 488 more genes
nsv6637531	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 100,334,135-110,383,902 , GRCh38.p12 chr13: 99,681,881-109,731,555	ARGLU1, LINC00343, 101 more genes
nsv6637400	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 97,142,120-115,107,733 , GRCh38.p12 chr13: 96,489,866-114,342,258	LOC107984609, LINC00354, 265 more genes
nsv6637217	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 99,421,603-115,107,733 , GRCh38.p12 chr13: 98,769,349-114,342,258	LOC107984609, CLYBL-AS2, 231 more genes
nsv6634431	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462	MTUS2-AS1, LOC105370213, 1330 more genes
nsv6621642	copy number variation	1	nstd224	human		GRCh37 chr13: 106,517,830-107,646,908 , GRCh38.p12 chr13: 105,865,481-106,994,560	LINC00460, ATP5MC1P5, 12 more genes
nsv6594777	inversion	1	nstd223	human		GRCh38 chr13: 104,930,881-106,737,596 , GRCh37.p13 chr13: 105,583,232-107,389,944	LINC00460, DAOA-AS1, 16 more genes
nsv6315552	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 89,490,345-115,062,235 , GRCh38.p12 chr13: 88,838,091-114,296,760	MIR20A, MIR548AR, 347 more genes
nsv6315495	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403	RNU6-80P, EFNB2, 1334 more genes
nsv6314171	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 79,370,012-115,107,733 , GRCh38.p12 chr13: 78,795,877-114,342,258	MIR4705, LOC102724149, 430 more genes
nsv6314066	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 100,258,328-115,107,733 , GRCh38.p12 chr13: 99,606,074-114,342,258	MIR4502, GRTP1-AS1, 208 more genes
nsv6314038	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 104,545,892-115,107,733 , GRCh38.p12 chr13: 103,893,542-114,342,258	LIG4, DAOA, 151 more genes
nsv6314030	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251	RPSAP53, LOC105370213, 1310 more genes
nsv6313971	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 85,037,147-115,107,733 , GRCh38.p12 chr13: 84,463,012-114,342,258	BRK1P2, UGGT2, 386 more genes
nsv6313904	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 78,514,567-115,107,733 , GRCh38.p12 chr13: 77,940,432-114,342,258	LOC101927284, LOC105370330, 444 more genes
nsv6291686	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr13: 106,041,961-107,588,983 , GRCh38.p12 chr13: 105,389,611-106,936,635	EFNB2, ARGLU1, 17 more genes
nsv6291487	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 42,504,540-108,206,269 , GRCh38.p12 chr13: 41,930,404-107,553,921	CALM2P4, RNU6-81P, 778 more genes

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Items: 1 to 20 of 205

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Number of Variants: 20

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