dbVar for Gene (Select 138799) - 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
nsv7148263	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 102,995,214-108,903,040 , GRCh37.p13 chr9: 105,757,496-111,665,320	ACTL7B, OR13C3, 88 more genes
nsv6876203	copy number variation	1	nstd229	human		GRCh38 chr9: 104,505,384-104,652,917 , GRCh37.p13 chr9: 107,267,665-107,415,198	OR13C4, OR13C8, 7 more genes
nsv6875429	copy number variation	1	nstd229	human		GRCh38 chr9: 104,598,501-104,605,800 , GRCh37.p13 chr9: 107,360,782-107,368,081	OR13C5, OR13C2
nsv6874535	copy number variation	1	nstd229	human		GRCh38 chr9: 104,597,601-104,605,800 , GRCh37.p13 chr9: 107,359,882-107,368,081	OR13C2, OR13C5
nsv6862067	copy number variation	1	nstd229	human		GRCh38 chr9: 104,598,301-104,605,800 , GRCh37.p13 chr9: 107,360,582-107,368,081	OR13C5, OR13C2
nsv6858959	copy number variation	1	nstd229	human		GRCh38 chr9: 104,599,647-104,605,764 , GRCh37.p13 chr9: 107,361,928-107,368,045	OR13C5, OR13C2
nsv6858842	copy number variation	1	nstd229	human		GRCh38 chr9: 104,599,601-104,605,800 , GRCh37.p13 chr9: 107,361,882-107,368,081	OR13C5, OR13C2
nsv6637573	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 106,173,402-107,431,515 , GRCh38.p12 chr9: 103,411,120-104,669,234	LOC105376194, TOPORSLP, 18 more genes
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
nsv6453336	copy number variation	1	nstd223	human		GRCh38 chr9: 104,588,061-104,612,601 , GRCh37.p13 chr9: 107,350,342-107,374,882	OR13D2P, OR13C5, 1 more genes
nsv6451013	copy number variation	1	nstd223	human		GRCh38 chr9: 104,599,201-104,600,100 , GRCh37.p13 chr9: 107,361,482-107,362,381	OR13C5
nsv6448405	copy number variation	1	nstd223	human		GRCh38 chr9: 104,505,382-104,652,916 , GRCh37.p13 chr9: 107,267,663-107,415,197	OR13I1P, OR13C5, 7 more genes
nsv6447734	copy number variation	1	nstd223	human		GRCh38 chr9: 104,596,801-104,597,800 , GRCh37.p13 chr9: 107,359,082-107,360,081	OR13C5
nsv6444882	copy number variation	1	nstd223	human		GRCh38 chr9: 104,599,630-104,605,739 , GRCh37.p13 chr9: 107,361,911-107,368,020	OR13C5, OR13C2
nsv6441632	copy number variation	1	nstd223	human		GRCh38 chr9: 104,598,621-104,604,835 , GRCh37.p13 chr9: 107,360,902-107,367,116	OR13C5, OR13C2
nsv6435839	copy number variation	1	nstd223	human		GRCh38 chr9: 104,599,601-104,605,400 , GRCh37.p13 chr9: 107,361,882-107,367,681	OR13C2, OR13C5
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
nsv6313900	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132	ABCA1, ALAD, 793 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
nsv6290765	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 102,858,276-110,624,997 , GRCh38.p12 chr9: 100,095,994-107,862,716	RNF20, SMC2, 120 more genes

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 178

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Number of Variants: 20

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