dbVar for Gene (Select 104326054) - 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
nsv7148164	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 106,425,676-114,326,445 , GRCh37.p13 chr13: 107,078,024-115,085,141	TUBGCP3, LINC01043, 132 more genes
nsv7065342	inversion	1	nstd229	human		GRCh38 chr13: 109,369,352-109,411,374 , GRCh37.p13 chr13: 110,021,699-110,063,721	LOC105370359, LINC00399
nsv7062466	inversion	1	nstd229	human		GRCh38 chr13: 107,288,249-110,580,799 , GRCh37.p13 chr13: 107,940,597-111,233,146	RNA5SP39, MIR1267, 32 more genes
nsv7060236	inversion	1	nstd229	human		GRCh38 chr13: 109,400,177-111,221,158 , GRCh37.p13 chr13: 110,052,524-111,873,505	LINC00399, ANKRD10, 36 more genes
nsv6951411	copy number variation	1	nstd229	human		GRCh38 chr13: 107,488,002-110,580,394 , GRCh37.p13 chr13: 108,140,350-111,232,741	LOC105370359, RN7SKP10, 30 more genes
nsv6945036	copy number variation	1	nstd229	human		GRCh38 chr13: 109,257,772-109,422,073 , GRCh37.p13 chr13: 109,910,120-110,074,420	LOC105370359, LINC00399
nsv6938111	copy number variation	1	nstd229	human		GRCh38 chr13: 109,247,401-109,678,300 , GRCh37.p13 chr13: 109,899,749-110,330,647	LOC105370359, LOC107984602, 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
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
nsv6314156	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 108,035,809-110,195,659 , GRCh38.p12 chr13: 107,383,461-109,543,312	MYO16, RNA5SP39, 14 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

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Has Clinical Interpretation

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Items: 1 to 20 of 210

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Number of Variants: 20

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