dbVar for Gene (Select 347275) - 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
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
nsv6858150	copy number variation	1	nstd229	human		GRCh38 chr9: 101,319,338-101,389,524 , GRCh37.p13 chr9: 104,081,620-104,151,806	LOC100421197, ACNATP, 5 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
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
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
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
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
nsv4982801	copy number variation	1	nstd200	human		GRCh38 chr9: 101,339,635-101,343,642 , GRCh37.p13 chr9: 104,101,917-104,105,924	ACNATP
nsv4824260	copy number variation	1	nstd200	human		GRCh37 chr9: 104,101,917-104,105,924 , GRCh38.p12 chr9\|NT_187578.1: 390,864-394,893 , GRCh38.p12 chr9: 101,339,635-101,343,642	ACNATP
nsv4728848	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 103,872,812-104,974,365 , GRCh38.p12 chr9: 101,110,530-102,212,083	RNF20, LOC105376184, 20 more genes
nsv4684256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991	RPS26P37, MIR27B, 238 more genes
nsv4479561	mobile element insertion	1	nstd166	human		GRCh37.p13 chr9: 104,097,726-104,097,726 , GRCh38.p12 chr9\|NT_187578.1: 386,647-386,647 , GRCh38.p12 chr9: 101,335,444-101,335,444	ACNATP
nsv4457273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936	CDRT15P14, MIR548AW, 2167 more genes
nsv4455186	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937	LOC105376327, ENG, 1304 more genes
nsv4337085	sequence alteration	1	nstd166	human		GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042	, ABCA1, 927 more genes
nsv3965731	insertion	1	nstd168	human		GRCh38 chr9: 101,312,824-101,364,606 , GRCh37.p13 chr9: 104,075,106-104,126,888	BAAT, PLPPR1, 3 more genes

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 109

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Number of Variants: 20

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