dbVar for Gene (Select 101928616) - 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
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
nsv7075459	inversion	1	nstd229	human		GRCh38 chr13: 110,952,781-112,398,036 , GRCh37.p13 chr13: 111,605,128-112,978,183	LOC102724489, LINC01044, 28 more genes
nsv7074580	inversion	1	nstd229	human		GRCh38 chr13: 110,243,158-113,630,621 , GRCh37.p13 chr13: 110,895,505-114,284,936	LINC01070, NAXD, 71 more genes
nsv6950561	copy number variation	1	nstd229	human		GRCh38 chr13: 111,894,891-111,899,566 , GRCh37.p13 chr13: 112,549,205-112,553,880	LINC00354
nsv6943198	copy number variation	1	nstd229	human		GRCh38 chr13: 111,028,013-113,621,089 , GRCh37.p13 chr13: 111,680,360-114,275,404	ARHGEF7, GRTP1, 52 more genes
nsv6942572	copy number variation	1	nstd229	human		GRCh38 chr13: 111,892,799-111,895,641 , GRCh37.p13 chr13: 112,547,113-112,549,955	LINC00354
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
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
nsv6621645	copy number variation	1	nstd224	human		GRCh37 chr13: 110,236,646-115,091,330 , GRCh38.p12 chr13: 109,584,299-114,325,855	PARP1P1, F7, 103 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
nsv6315465	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 110,428,062-115,107,733 , GRCh38.p12 chr13: 109,775,715-114,342,258	SALL4P4, KARS1P2, 103 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

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 235

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Number of Variants: 20

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