dbVar for Gene (Select 286359) - 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
nsv7075365	inversion	1	nstd229	human		GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272	PCAT7, ANKS6, 128 more genes
nsv6871281	copy number variation	1	nstd229	human		GRCh38 chr9: 97,389,945-97,393,256 , GRCh37.p13 chr9: 100,152,227-100,155,538	LOC286359
nsv6861096	copy number variation	1	nstd229	human		GRCh38 chr9: 97,302,701-97,408,400 , GRCh37.p13 chr9: 100,064,983-100,170,682	LOC286359, CCDC180, 2 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
nsv6447755	copy number variation	1	nstd223	human		GRCh38 chr9: 92,901,749-100,255,234 , GRCh37.p13 chr9: 95,664,031-103,017,516	EIF4BP3, VN1R51P, 162 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
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
nsv6136854	copy number variation	1	nstd213	human		GRCh37 chr9: 99,740,000-100,170,001 , GRCh38.p12 chr9: 96,977,718-97,407,719	SUGT1P4-STRA6LP-CCDC180, MFSD14CP, 19 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
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
nsv4676103	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 95,946,863-99,986,314 , GRCh37.p13 chr9: 96,907,042-100,946,493 , GRCh38.p12 chr9: 94,144,760-98,184,211	MIR3074, LOC112268039, 108 more genes
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
nsv3922790	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 94,713,892-98,121,186 , GRCh37 chr9: 97,476,174-100,883,468 , NCBI36 chr9: 96,515,995-99,923,289	CDC14B, PTCH1, 87 more genes
nsv3922685	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 88,522,292-113,687,796 , NCBI36 chr9: 90,327,027-115,489,897 , GRCh37 chr9: 91,137,207-116,450,076	MUSK, LOC105376176, 464 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	TDRD7, CDK9, 2170 more genes

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Items: 1 to 20 of 99

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Number of Variants: 20

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