dbVar for Gene (Select 10912) - 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
nsv4887530	inversion	1	nstd200	human		GRCh37 chr9: 90,662,371-96,951,001 , GRCh38.p12 chr9: 88,047,456-94,188,719	, MTATP6P29, 125 more genes
nsv4729419	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 90,031,614-93,173,691 , GRCh38.p12 chr9: 87,416,699-90,411,409	CKS2, CTSL, 60 more genes
nsv4674876	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 90,002,910-94,567,835 , GRCh38.p12 chr9: 87,387,995-91,805,553	AUH, CKS2, 78 more genes
nsv4668305	copy number variation	1	nstd186	human		GRCh37 chr9: 91,963,403-92,343,382 , GRCh38.p12 chr9: 89,348,488-89,728,467	, SEMA4D, 7 more genes
nsv4605177	copy number variation	2	nstd183	human		GRCh37 chr9: 91,963,403-92,343,382 , GRCh38.p12 chr9: 89,348,488-89,728,467	, GADD45G, 8 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
nsv4349215	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 79,520,825-97,201,274 , GRCh38.p12 chr9: 76,905,909-94,438,992	SPATA31C1, LINC02893, 280 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
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
nsv3921598	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389	PGAP4, ECPAS, 2167 more genes
nsv3920967	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 89,223,315-92,208,114 , GRCh38 chr9: 87,418,580-90,406,012 , GRCh37 chr9: 90,033,495-93,168,294	LOC105376131, LOC107987091, 60 more genes
nsv3920713	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389	ABHD17B, LOC100533707, 2167 more genes
nsv3919257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718	LOC107987031, LOC105376234, 2169 more genes
nsv3917022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 214,367-141,008,915 , GRCh38 chr9: 193,412-138,114,463 , NCBI36 chr9: 204,367-140,128,736	RN7SKP87, SPATA6L, 2168 more genes
nsv3915973	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346	CTNNAL1, QSOX2, 2170 more genes
nsv3915533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 88,694,766-94,589,503 , NCBI36 chr9: 87,884,586-93,629,324 , GRCh38 chr9: 86,079,851-91,827,221	SPIN1, PAICSP2, 98 more genes
nsv3914702	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 71,130,848-109,341,774 , NCBI36 chr9: 70,225,166-108,381,595 , GRCh38 chr9: 68,420,430-106,579,493	CDCA7P2, ASPN, 603 more genes
nsv3912247	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981	ALOX15P2, LOC107987061, 2184 more genes

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Number of Variants: 20

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Items: 1 to 20 of 94

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Number of Variants: 20

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