dbVar for Gene (Select 93081) - 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
nsv7098899	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 95,675,427-105,286,434 , GRCh38.p12 chr13: 95,023,173-104,634,083	PCCA, LOC105370340, 131 more genes
nsv7094230	copy number variation	3	nstd102	human	Uncertain significance	GRCh37 chr13: 100,038,233-103,718,599 , GRCh38.p12 chr13: 99,385,979-103,066,249	CLYBL-AS3, LOC107984615, 59 more genes
nsv7094066	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 102,521,055-103,718,599 , GRCh38.p12 chr13: 101,868,705-103,066,249	FGF14-AS1, POGLUT2, 22 more genes
nsv7077072	inversion	1	nstd229	human		GRCh38 chr13: 102,676,907-102,874,566 , GRCh37.p13 chr13: 103,329,257-103,526,916	CCDC168, POGLUT2, 8 more genes
nsv7072178	inversion	1	nstd229	human		GRCh38 chr13: 97,997,035-104,548,310 , GRCh37.p13 chr13: 98,649,289-105,200,661	RNU1-24P, DOCK9, 95 more genes
nsv6953254	copy number variation	1	nstd229	human		GRCh38 chr13: 102,762,471-102,769,376 , GRCh37.p13 chr13: 103,414,821-103,421,726	LOC105370337, TEX30
nsv6945936	copy number variation	1	nstd229	human		GRCh38 chr13: 102,668,892-102,872,921 , GRCh37.p13 chr13: 103,321,242-103,525,271	RNY5P8, TPP2, 8 more genes
nsv6943989	copy number variation	1	nstd229	human		GRCh38 chr13: 102,764,435-102,768,743 , GRCh37.p13 chr13: 103,416,785-103,421,093	LOC105370337, TEX30
nsv6942971	copy number variation	1	nstd229	human		GRCh38 chr13: 102,773,343-102,779,210 , GRCh37.p13 chr13: 103,425,693-103,431,560	TEX30
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
nsv6637615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 93,535,335-105,788,229 , GRCh38.p12 chr13: 92,883,082-105,135,878	SNORD13G, FTLP8, 162 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
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

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Number of Variants: 20

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 194

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Number of Variants: 20

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