dbVar for Gene (Select 653404) - 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
nsv6634454	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944	HNRNPA1P41, GAS1RR, 1868 more genes
nsv6633539	copy number variation	1	nstd224	human		GRCh37 chr9: 69,033,702-69,257,427 , GRCh38.p12 chr9: 40,960,473-41,184,198	LINC03025, PGM5P2, 5 more genes
nsv6454051	copy number variation	1	nstd223	human		GRCh38 chr9: 41,052,901-41,129,400 , GRCh37.p13 chr9: 69,126,130-69,202,629	LOC105376058, LINC03025, 3 more genes
nsv6450978	copy number variation	1	nstd223	human		GRCh38 chr9: 41,053,401-41,142,900 , GRCh37.p13 chr9: 69,126,630-69,216,129	LOC105376058, LINC03025, 3 more genes
nsv6449928	copy number variation	1	nstd223	human		GRCh38 chr9: 41,124,401-41,125,600 , GRCh37.p13 chr9: 69,197,630-69,198,829	LINC03025, FOXD4L6
nsv6449063	copy number variation	1	nstd223	human		GRCh38 chr9: 41,049,601-41,226,000 , GRCh37.p13 chr9: 69,122,830-69,278,385	PGM5P2, LOC105376058, 4 more genes
nsv6447639	copy number variation	1	nstd223	human		GRCh38 chr9: 41,054,101-41,128,000 , GRCh37.p13 chr9: 69,127,330-69,201,229	FOXD4L6, LINC03025, 2 more genes
nsv6445227	copy number variation	1	nstd223	human		GRCh38 chr9: 40,876,369-41,152,593 , GRCh37.p13 chr9: 68,664,183-68,838,946	PGM5P2, FRG1HP, 6 more genes
nsv6443882	copy number variation	1	nstd223	human		GRCh38 chr9: 41,049,801-41,130,700 , GRCh37.p13 chr9: 69,123,030-69,203,929	LOC105376058, LINC03025, 3 more genes
nsv6442911	copy number variation	1	nstd223	human		GRCh38 chr9: 41,123,701-41,125,300 , GRCh37.p13 chr9: 69,196,930-69,198,529	LINC03025, FOXD4L6
nsv6441227	copy number variation	1	nstd223	human		GRCh38 chr9: 41,126,701-41,127,700 , GRCh37.p13 chr9: 69,199,930-69,200,929	FOXD4L6
nsv6436428	copy number variation	1	nstd223	human		GRCh38 chr9: 41,052,801-41,128,300 , GRCh37.p13 chr9: 69,126,030-69,201,529	PGM5P2, LOC105376058, 2 more genes
nsv6315415	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552	LOC107987068, FAM74A7, 846 more genes
nsv6315405	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032	RNU6-156P, GDA, 1425 more genes
nsv6313827	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484	RPSAP75, ANKRD20A2P, 1008 more genes
nsv6313546	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937	FAM27C, DPM2, 2166 more genes
nsv6290004	inversion	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378	ACO1, PLIN2, 1215 more genes
nsv6142522	copy number variation	1	nstd206	human		GRCh38 chr9: 40,561,974-41,135,974 , GRCh37.p13 chr: NaN-NaN	IGKV1OR9-2, FOXD4L6, 14 more genes
nsv5911060	copy number variation	1	nstd209	human		GRCh38 chr9: 40,229,279-42,858,473 , GRCh37.p13 chr9: 42,792,885-46,287,854	, LOC107984035, 69 more genes
nsv5909117	copy number variation	1	nstd209	human		GRCh38 chr9: 40,903,761-43,206,180 , GRCh37.p13 chr9: 40,029,241-41,240,039	, LOC100420440, 62 more genes

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Number of Variants: 20

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Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 417

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Number of Variants: 20

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