dbVar for Gene (Select 10367) - 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
nsv7143660	insertion	1	nstd232	human		GRCh37.p13 chr10: 74,311,099-74,311,099 , GRCh38.p12 chr10: 72,551,341-72,551,341	MICU1
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
nsv7098904	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 72,485,363-72,566,418 , GRCh37.p13 chr10: 74,245,121-74,326,176	MICU1
nsv7093800	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 74,322,633-74,322,841 , GRCh38.p12 chr10: 72,562,875-72,563,083	MICU1
nsv7093799	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 74,182,972-74,326,551 , GRCh38.p12 chr10: 72,423,214-72,566,793	MICU1, SNX19P4
nsv7093729	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 74,167,667-74,183,149 , GRCh38.p12 chr10: 72,407,909-72,423,391	MICU1
nsv7093648	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 74,322,633-74,326,551 , GRCh38.p12 chr10: 72,562,875-72,566,793	MICU1
nsv7093647	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 74,135,521-74,326,551 , GRCh38.p12 chr10: 72,375,763-72,566,793	SNX19P4, MICU1, 1 more genes
nsv7076198	inversion	1	nstd229	human		GRCh38 chr10: 72,402,166-72,588,053 , GRCh37.p13 chr10: 74,161,924-74,347,811	SNX19P4, MICU1, 1 more genes
nsv7070912	inversion	1	nstd229	human		GRCh38 chr10: 72,459,508-72,494,603 , GRCh37.p13 chr10: 74,219,266-74,254,361	MICU1, SNX19P4
nsv7063446	inversion	1	nstd229	human		GRCh38 chr10: 72,571,840-72,575,136 , GRCh37.p13 chr10: 74,331,598-74,334,894	MICU1
nsv7062735	inversion	1	nstd229	human		GRCh38 chr10: 72,428,568-72,459,669 , GRCh37.p13 chr10: 74,188,326-74,219,427	MICU1
nsv7058811	inversion	1	nstd229	human		GRCh38 chr10: 72,574,887-72,582,226 , GRCh37.p13 chr10: 74,334,645-74,341,984	RN7SL840P, MICU1
nsv6897465	copy number variation	1	nstd229	human		GRCh38 chr10: 72,493,592-72,507,786 , GRCh37.p13 chr10: 74,253,350-74,267,544	MICU1
nsv6897424	copy number variation	1	nstd229	human		GRCh38 chr10: 72,484,521-72,484,870 , GRCh37.p13 chr10: 74,244,279-74,244,628	MICU1
nsv6896193	copy number variation	1	nstd229	human		GRCh38 chr10: 72,429,101-72,440,900 , GRCh37.p13 chr10: 74,188,859-74,200,658	MICU1
nsv6895839	copy number variation	1	nstd229	human		GRCh38 chr10: 72,546,873-72,549,288 , GRCh37.p13 chr10: 74,306,631-74,309,046	MICU1
nsv6895764	copy number variation	1	nstd229	human		GRCh38 chr10: 72,130,486-72,490,292 , GRCh37.p13 chr10: 73,890,244-74,250,050	SNX19P4, ASCC1, 6 more genes
nsv6895621	copy number variation	1	nstd229	human		GRCh38 chr10: 72,564,499-72,567,888 , GRCh37.p13 chr10: 74,324,257-74,327,646	MICU1

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Study Type

Subject Phenotype Status

Additional filters

Links from Gene

Items: 1 to 20 of 851

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Number of Variants: 20

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