dbVar for Gene (Select 64421) - 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
nsv7137211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639	EXOC6, VCL, 1906 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	RNU7-12P, RNU1-65P, 1876 more genes
nsv7093869	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 14,991,015-14,991,106 , GRCh38.p12 chr10: 14,949,016-14,949,107	DCLRE1C
nsv7093868	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 14,976,682-14,996,009 , GRCh38.p12 chr10: 14,934,683-14,954,010	MEIG1, DCLRE1C
nsv7093867	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 14,976,359-14,996,009 , GRCh38.p12 chr10: 14,934,360-14,954,010	DCLRE1C, MEIG1
nsv7093785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 14,977,442-14,996,029 , GRCh38.p12 chr10: 14,935,443-14,954,030	MEIG1, DCLRE1C
nsv7093709	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 14,987,084-14,996,009 , GRCh38.p12 chr10: 14,945,085-14,954,010	MEIG1, DCLRE1C
nsv7093708	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr10: 14,981,799-14,981,878 , GRCh38.p12 chr10: 14,939,800-14,939,879	DCLRE1C
nsv7093628	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 14,981,799-14,996,009 , GRCh38.p12 chr10: 14,939,800-14,954,010	MEIG1, DCLRE1C
nsv7093627	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 14,976,692-14,996,009 , GRCh38.p12 chr10: 14,934,693-14,954,010	DCLRE1C, MEIG1
nsv7093506	insertion	1	nstd102	human	Pathogenic	GRCh37 chr10: 14,951,239-14,951,239 , GRCh38 chr10: 14,909,240-14,909,240	DCLRE1C
nsv7093505	insertion	1	nstd102	human	Pathogenic	GRCh37 chr10: 14,950,996-14,950,996 , GRCh38 chr10: 14,908,997-14,908,997	DCLRE1C
nsv7093423	delins	1	nstd102	human	Pathogenic	GRCh37 chr10: 14,951,238-14,951,238 , GRCh38 chr10: 14,909,239-14,909,239	DCLRE1C
nsv7093356	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 14,934,776-14,939,809 , GRCh37.p13 chr10: 14,976,775-14,981,808	DCLRE1C
nsv7060184	inversion	1	nstd229	human		GRCh38 chr10: 13,148,010-16,128,795 , GRCh37.p13 chr10: 13,190,010-16,170,794	LOC101928453, MCM10, 52 more genes
nsv6888778	copy number variation	1	nstd229	human		GRCh38 chr10: 14,935,906-15,023,266 , GRCh37.p13 chr10: 14,977,905-15,065,265	OR7E110P, DCLRE1C, 5 more genes
nsv6883208	copy number variation	1	nstd229	human		GRCh38 chr10: 14,941,319-14,945,348 , GRCh37.p13 chr10: 14,983,318-14,987,347	DCLRE1C
nsv6882586	copy number variation	1	nstd229	human		GRCh38 chr10: 14,934,791-14,938,650 , GRCh37.p13 chr10: 14,976,790-14,980,649	DCLRE1C
nsv6635468	copy number variation	1	nstd227	human		GRCh38.p12 chr10: 14,945,441-15,018,884 , GRCh37 chr10: 14,987,440-15,060,883	DCLRE1C, OR7E115P, 5 more genes
nsv6634685	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 14,983,601-15,065,700 , GRCh38.p12 chr10: 14,941,602-15,023,701	DCLRE1C, OR7E115P, 5 more genes

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Number of Variants: 20

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Organism

Variant Type

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Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 364

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Number of Variants: 20

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