dbVar for Gene (Select 100133036) - 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
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
nsv6315415	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552	LOC107987068, FAM74A7, 846 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
nsv6313827	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484	RPSAP75, ANKRD20A2P, 1008 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
nsv6142454	copy number variation	1	nstd206	human		GRCh38 chr9: 40,284,000-40,431,400 , GRCh37.p13 chr9: 42,429,018-42,576,418	FAM95B1, SNX18P8, 3 more genes
nsv5911060	copy number variation	1	nstd209	human		GRCh38 chr9: 40,229,279-42,858,473 , GRCh37.p13 chr9: 42,792,885-46,287,854	, LOC107984035, 69 more genes
nsv5664563	inversion	1	nstd207	human		GRCh38 chr9: 39,265,868-42,796,744 , GRCh37.p13 chr9: 42,792,885-46,287,854	, PTGER4P1, 95 more genes
nsv5554508	sequence alteration	1	nstd206	human		GRCh38 chr9: 39,866,147-63,791,228 , GRCh37.p13 chr9: 39,713,687-67,542,104	, PTGER4P2, 168 more genes
nsv5539488	insertion	1	nstd206	human		GRCh38 chr9: 40,322,247-40,322,256 , GRCh37.p13 chr9: 42,467,265-42,467,274	FAM95B1
nsv5254971	copy number variation	1	nstd204	human		GRCh38.p13 chr9: 40,328,601-40,342,000 , GRCh37.p13 chr9: 42,473,619-42,487,018	LOC100419690, FAM95B1
nsv4766654	inversion	1	nstd199	human		GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552	, ACO1, 876 more genes
nsv4755256	inversion	1	nstd199	human		GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552	, ACO1, 876 more genes
nsv4730044	inversion	33	nstd198	human		GRCh38 chr9: 39,599,468-41,573,547 , GRCh37.p13 chr: NaN-NaN	, PTGER4P1, 59 more genes
nsv4675565	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672	LOC100132004, LOC105375993, 853 more genes
nsv4647995	copy number variation	4	nstd186	human		GRCh37 chr9: 42,471,350-42,481,000 , GRCh38.p12 chr9: 40,326,332-40,335,982	FAM95B1, LOC100419690
nsv4608528	copy number variation	2	nstd183	human		GRCh37 chr9: 42,438,251-42,469,994 , GRCh38.p12 chr9: 40,293,233-40,324,976	FAM95B1, SNX18P8
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
nsv4457200	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-67,986,965 , GRCh38.p12 chr9: 203,861-67,919,519	ACO1, RNU6-1073P, 846 more genes

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Number of Variants: 20

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Object Type

Organism

Variant Type

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 152

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Number of Variants: 20

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