dbVar for Gene (Select 9124) - 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
nsv7098887	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213	LGI1, LOC107984257, 79 more genes
nsv7060443	inversion	1	nstd229	human		GRCh38 chr10: 94,671,513-95,794,260 , GRCh37.p13 chr10: 96,431,270-97,554,017	ENTPD1, RPL7AP52, 20 more genes
nsv6897820	copy number variation	1	nstd229	human		GRCh38 chr10: 95,261,401-95,268,100 , GRCh37.p13 chr10: 97,021,158-97,027,857	PDLIM1
nsv6896964	copy number variation	1	nstd229	human		GRCh38 chr10: 95,289,333-95,289,446 , GRCh37.p13 chr10: 97,049,090-97,049,203	PDLIM1
nsv6896357	copy number variation	1	nstd229	human		GRCh38 chr10: 95,152,977-95,236,014 , GRCh37.p13 chr10: 96,912,734-96,995,771	PDLIM1, ACSM6, 2 more genes
nsv6896107	copy number variation	1	nstd229	human		GRCh38 chr10: 94,375,560-95,464,831 , GRCh37.p13 chr10: 96,135,317-97,224,588	SORBS1, MTND4P19, 18 more genes
nsv6895244	copy number variation	1	nstd229	human		GRCh38 chr10: 95,250,840-95,255,133 , GRCh37.p13 chr10: 97,010,597-97,014,890	PDLIM1
nsv6894381	copy number variation	1	nstd229	human		GRCh38 chr10: 95,276,533-95,279,376 , GRCh37.p13 chr10: 97,036,290-97,039,133	PDLIM1
nsv6888814	copy number variation	1	nstd229	human		GRCh38 chr10: 95,247,390-95,288,233 , GRCh37.p13 chr10: 97,007,147-97,047,990	PDLIM1
nsv6888655	copy number variation	1	nstd229	human		GRCh38 chr10: 95,242,215-95,246,742 , GRCh37.p13 chr10: 97,001,972-97,006,499	PDLIM1
nsv6888484	copy number variation	1	nstd229	human		GRCh38 chr10: 95,259,811-95,268,784 , GRCh37.p13 chr10: 97,019,568-97,028,541	PDLIM1
nsv6886873	copy number variation	1	nstd229	human		GRCh38 chr10: 95,281,308-95,282,669 , GRCh37.p13 chr10: 97,041,065-97,042,426	PDLIM1
nsv6883599	copy number variation	1	nstd229	human		GRCh38 chr10: 95,284,340-95,284,678 , GRCh37.p13 chr10: 97,044,097-97,044,435	PDLIM1
nsv6882971	copy number variation	1	nstd229	human		GRCh38 chr10: 95,280,165-95,286,426 , GRCh37.p13 chr10: 97,039,922-97,046,183	PDLIM1
nsv6881213	copy number variation	1	nstd229	human		GRCh38 chr10: 95,278,439-95,283,597 , GRCh37.p13 chr10: 97,038,196-97,043,354	PDLIM1
nsv6879849	copy number variation	1	nstd229	human		GRCh38 chr10: 95,238,687-95,247,217 , GRCh37.p13 chr10: 96,998,444-97,006,974	PDLIM1
nsv6637999	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 96,155,285-97,224,160 , GRCh38.p12 chr10: 94,395,528-95,464,403	CYP2C58P, CTBP2P2, 18 more genes
nsv6595106	inversion	1	nstd223	human		GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244	, ARHGAP19, 201 more genes

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Number of Variants: 20

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Organism

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Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 257

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Number of Variants: 20

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