dbVar for Gene (Select 253970) - 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
nsv7094498	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 36,988,170-36,989,334 , GRCh38.p12 chr14: 36,518,965-36,520,129	SFTA3, NKX2-1-AS1, 1 more genes
nsv7077983	inversion	1	nstd229	human		GRCh38 chr14: 36,470,974-36,488,156 , GRCh37.p13 chr14: 36,940,179-36,957,361	SFTA3
nsv7073782	inversion	1	nstd229	human		GRCh38 chr14: 36,480,656-36,487,924 , GRCh37.p13 chr14: 36,949,861-36,957,129	SFTA3
nsv7072225	inversion	1	nstd229	human		GRCh38 chr14: 31,291,623-36,485,208 , GRCh37.p13 chr14: 31,760,829-36,954,413	LOC101927178, RNU7-93P, 84 more genes
nsv6957449	copy number variation	1	nstd229	human		GRCh38 chr14: 36,482,086-36,508,369 , GRCh37.p13 chr14: 36,951,291-36,977,574	SFTA3
nsv6956783	copy number variation	1	nstd229	human		GRCh38 chr14: 36,512,101-36,527,500 , GRCh37.p13 chr14: 36,981,306-36,996,705	NKX2-1, LOC105370453, 2 more genes
nsv6953707	copy number variation	1	nstd229	human		GRCh38 chr14: 36,464,132-36,486,447 , GRCh37.p13 chr14: 36,933,337-36,955,652	SFTA3
nsv6941451	copy number variation	1	nstd229	human		GRCh38 chr14: 36,516,745-36,517,316 , GRCh37.p13 chr14: 36,985,950-36,986,521	NKX2-1-AS1, NKX2-1, 1 more genes
nsv6622519	copy number variation	1	nstd224	human		GRCh37 chr14: 36,916,520-37,243,034 , GRCh38.p12 chr14: 36,447,315-36,773,829	PAX9, SLC25A21, 9 more genes
nsv6590381	inversion	1	nstd223	human		GRCh38 chr14: 36,470,971-36,488,156 , GRCh37.p13 chr14: 36,940,176-36,957,361	SFTA3
nsv6491914	copy number variation	1	nstd223	human		GRCh38 chr14: 36,506,958-36,507,795 , GRCh37.p13 chr14: 36,976,163-36,977,000	SFTA3
nsv6315513	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000	CDH24, KLHL33, 623 more genes
nsv6314715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884	HNRNPC, FOXG1, 616 more genes
nsv6313989	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 36,924,877-37,247,672 , GRCh38.p12 chr14: 36,455,672-36,778,467	NKX2-8, PAX9, 9 more genes
nsv6313950	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 36,933,561-37,247,672 , GRCh38.p12 chr14: 36,464,356-36,778,467	NKX2-1, RPL29P3, 9 more genes
nsv6313916	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 36,862,276-41,597,549 , GRCh38.p12 chr14: 36,393,071-41,128,344	LOC105370462, LOC105370459, 55 more genes
nsv6309692	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 36,986,483-36,987,245 , GRCh38.p12 chr14: 36,517,278-36,518,040	NKX2-1, SFTA3, 1 more genes
nsv6309545	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 36,986,483-37,228,504 , GRCh38.p12 chr14: 36,517,278-36,759,299	LOC105370455, PHKBP2, 9 more genes
nsv6133125	copy number variation	1	nstd213	human		GRCh37 chr14: 36,260,000-37,190,001 , GRCh38.p12 chr14: 35,790,794-36,720,796	MBIP, LOC644584, 22 more genes
nsv6106211	inversion	1	nstd212	human		GRCh38 chr14: 35,414,234-38,834,329 , GRCh37.p13 chr14: 35,883,440-39,303,533	, FOXA1, 49 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 204

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Number of Variants: 20

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