dbVar for Gene (Select 27199) - 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
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
nsv7077440	inversion	1	nstd229	human		GRCh38 chr13: 95,324,680-102,597,006 , GRCh37.p13 chr13: 95,976,934-103,249,356	RN7SL60P, RPL15P18, 111 more genes
nsv6951071	copy number variation	1	nstd229	human		GRCh38 chr13: 96,013,973-97,010,882 , GRCh37.p13 chr13: 96,666,227-97,663,136	AMMECR1LP1, HSP90AB6P, 8 more genes
nsv6943532	copy number variation	1	nstd229	human		GRCh38 chr13: 96,915,892-97,019,911 , GRCh37.p13 chr13: 97,568,146-97,672,165	LINC00359, RN7SKP7, 2 more genes
nsv6939189	copy number variation	1	nstd229	human		GRCh38 chr13: 96,994,402-96,998,382 , GRCh37.p13 chr13: 97,646,656-97,650,636	OXGR1
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
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
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
nsv6488448	copy number variation	1	nstd223	human		GRCh38 chr13: 96,013,973-97,010,882 , GRCh37.p13 chr13: 96,666,227-97,663,136	UGGT2, RN7SKP7, 8 more genes
nsv6482033	copy number variation	1	nstd223	human		GRCh38 chr13: 96,947,487-97,018,801 , GRCh37.p13 chr13: 97,599,741-97,671,055	RN7SKP7, OXGR1, 2 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
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
nsv6291748	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 97,387,902-97,732,153 , GRCh38.p12 chr13: 96,735,648-97,079,899	LINC00359, OXGR1, 4 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
nsv6289999	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403	LINC00363, LOC105370118, 1334 more genes

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Items: 1 to 20 of 177

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Number of Variants: 20

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