dbVar for Gene (Select 56254) - 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
nsv7145586	insertion	1	nstd232	human		GRCh37.p13 chr9: 104,313,898-104,313,898 , GRCh38.p12 chr9: 101,551,616-101,551,616	RNF20
nsv7097677	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 104,124,710-104,500,261 , GRCh38.p12 chr9: 101,362,428-101,737,979	TMEM246-AS1, PGAP4, 10 more genes
nsv6868418	copy number variation	1	nstd229	human		GRCh38 chr9: 101,302,335-101,603,079 , GRCh37.p13 chr9: 104,064,617-104,365,361	RNF20, PLPPR1, 14 more genes
nsv6860397	copy number variation	1	nstd229	human		GRCh38 chr9: 101,549,595-101,841,268 , GRCh37.p13 chr9: 104,311,877-104,603,550	GRIN3A, LOC105376186, 4 more genes
nsv6860201	copy number variation	1	nstd229	human		GRCh38 chr9: 101,540,892-101,541,019 , GRCh37.p13 chr9: 104,303,174-104,303,301	RNF20
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
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
nsv6315179	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300	SUGT1P4-STRA6LP, NR4A3, 255 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
nsv6209583	insertion	1	nstd214	human		GRCh38 chr9: 101,551,616-101,551,616 , GRCh37.p13 chr9: 104,313,898-104,313,898	RNF20
nsv6136627	copy number variation	1	nstd213	human		GRCh37 chr9: 104,030,000-104,350,001 , GRCh38.p12 chr9: 101,267,718-101,587,719	ALDOB, BAAT, 12 more genes
nsv6083308	insertion	1	nstd212	human		GRCh38 chr9: 101,551,616-101,551,616 , GRCh37.p13 chr9: 104,313,898-104,313,898	RNF20
nsv5949856	insertion	1	nstd209	human		GRCh38 chr9: 101,551,616-101,551,616 , GRCh37.p13 chr9: 104,313,898-104,313,898	RNF20
nsv5626919	insertion	1	nstd207	human		GRCh38 chr9: 101,551,616-101,551,616 , GRCh37.p13 chr9: 104,313,898-104,313,898	RNF20
nsv5546643	insertion	1	nstd206	human		GRCh38 chr9: 101,551,618-101,551,667 , GRCh37.p13 chr9: 104,313,900-104,313,949	RNF20
nsv5381561	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807	TBC1D2, ZNF782, 170 more genes
nsv5122220	mobile element insertion	1	nstd203	human		GRCh38 chr9: 101,561,616-101,561,629 , GRCh37.p13 chr9: 104,323,898-104,323,911	RNF20
nsv5040732	inversion	1	nstd200	human		GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990	, LOC105379839, 440 more genes

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Number of Variants: 20

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Items: 1 to 20 of 153

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Number of Variants: 20

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