dbVar for Gene (Select 56521) - 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
nsv7139479	insertion	1	nstd232	human		GRCh37.p13 chr10: 69,585,413-69,585,413 , GRCh38.p12 chr10: 67,825,655-67,825,655	DNAJC12, RN7SL394P
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
nsv7065859	inversion	1	nstd229	human		GRCh38 chr10: 67,827,831-67,827,905 , GRCh37.p13 chr10: 69,587,589-69,587,663	DNAJC12
nsv6897946	copy number variation	1	nstd229	human		GRCh38 chr10: 67,795,106-67,804,331 , GRCh37.p13 chr10: 69,554,864-69,564,089	DNAJC12
nsv6895012	copy number variation	1	nstd229	human		GRCh38 chr10: 67,784,939-67,795,566 , GRCh37.p13 chr10: 69,544,697-69,555,324	RPL21P92, DNAJC12
nsv6884305	copy number variation	1	nstd229	human		GRCh38 chr10: 67,797,894-67,798,537 , GRCh37.p13 chr10: 69,557,652-69,558,295	DNAJC12
nsv6882629	copy number variation	1	nstd229	human		GRCh38 chr10: 67,812,601-67,893,800 , GRCh37.p13 chr10: 69,572,359-69,653,558	DNAJC12, SIRT1, 4 more genes
nsv6880952	copy number variation	1	nstd229	human		GRCh38 chr10: 67,816,869-67,817,271 , GRCh37.p13 chr10: 69,576,627-69,577,029	DNAJC12
nsv6879964	copy number variation	1	nstd229	human		GRCh38 chr10: 67,751,501-67,942,800 , GRCh37.p13 chr10: 69,511,259-69,702,557	RN7SL394P, RNU6-1250P, 9 more genes
nsv6637501	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 69,575,390-69,911,592 , GRCh38.p12 chr10: 67,815,632-68,151,835	RN7SL220P, HERC4, 10 more genes
nsv6588588	inversion	1	nstd223	human		GRCh38 chr10: 67,798,445-67,798,796 , GRCh37.p13 chr10: 69,558,203-69,558,554	DNAJC12
nsv6586544	inversion	1	nstd223	human		GRCh38 chr10: 67,824,081-67,824,880 , GRCh37.p13 chr10: 69,583,839-69,584,638	DNAJC12, RN7SL394P
nsv6577702	inversion	1	nstd223	human		GRCh38 chr10: 67,818,744-67,819,160 , GRCh37.p13 chr10: 69,578,502-69,578,918	DNAJC12
nsv6576046	inversion	1	nstd223	human		GRCh38 chr10: 67,820,927-67,821,305 , GRCh37.p13 chr10: 69,580,685-69,581,063	DNAJC12
nsv6437577	copy number variation	1	nstd223	human		GRCh38 chr10: 67,799,701-67,800,800 , GRCh37.p13 chr10: 69,559,459-69,560,558	DNAJC12
nsv6436499	copy number variation	1	nstd223	human		GRCh38 chr10: 67,797,896-67,798,509 , GRCh37.p13 chr10: 69,557,654-69,558,267	DNAJC12
nsv6314185	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956	SLC25A16, CTNNA3, 204 more genes
nsv6309001	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 69,556,874-69,565,565 , GRCh38.p12 chr10: 67,797,116-67,805,807	DNAJC12
nsv6308916	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 67,680,088-71,332,799 , GRCh38.p12 chr10: 65,920,330-69,573,043	RPS3AP38, MIR7151, 62 more genes

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Number of Variants: 20

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Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 255

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Number of Variants: 20

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