dbVar for Gene (Select 7222) - 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
nsv7096974	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 121,616,266-124,323,706 , GRCh38.p12 chr4: 120,695,111-123,402,551	RN7SL335P, QRFPR, 40 more genes
nsv7046043	inversion	1	nstd229	human		GRCh38 chr4: 121,571,489-125,148,298 , GRCh37.p13 chr4: 122,492,644-126,069,453	TRC-GCA2-1, LINC02435, 39 more genes
nsv7043432	inversion	1	nstd229	human		GRCh38 chr4: 117,041,189-125,064,058 , GRCh37.p13 chr4: 117,962,345-125,985,213	SEPTIN14P4, LINC02516, 109 more genes
nsv6757380	copy number variation	1	nstd229	human		GRCh38 chr4: 121,949,701-122,005,400 , GRCh37.p13 chr4: 122,870,856-122,926,555	LOC102724158, TRPC3
nsv6755603	copy number variation	1	nstd229	human		GRCh38 chr4: 121,914,855-121,924,290 , GRCh37.p13 chr4: 122,836,010-122,845,445	TRPC3
nsv6755488	copy number variation	1	nstd229	human		GRCh38 chr4: 121,880,037-121,932,189 , GRCh37.p13 chr4: 122,801,192-122,853,344	TRPC3
nsv6754611	copy number variation	1	nstd229	human		GRCh38 chr4: 121,883,601-121,927,000 , GRCh37.p13 chr4: 122,804,756-122,848,155	TRPC3
nsv6752706	copy number variation	1	nstd229	human		GRCh38 chr4: 121,927,079-121,927,246 , GRCh37.p13 chr4: 122,848,234-122,848,401	TRPC3
nsv6751741	copy number variation	1	nstd229	human		GRCh38 chr4: 121,924,431-121,928,160 , GRCh37.p13 chr4: 122,845,586-122,849,315	TRPC3
nsv6750163	copy number variation	1	nstd229	human		GRCh38 chr4: 121,934,936-121,935,085 , GRCh37.p13 chr4: 122,856,091-122,856,240	TRPC3
nsv6744412	copy number variation	1	nstd229	human		GRCh38 chr4: 121,917,014-121,922,222 , GRCh37.p13 chr4: 122,838,169-122,843,377	TRPC3
nsv6742296	copy number variation	1	nstd229	human		GRCh38 chr4: 121,897,340-121,898,236 , GRCh37.p13 chr4: 122,818,495-122,819,391	TRPC3
nsv6741131	copy number variation	1	nstd229	human		GRCh38 chr4: 121,884,568-121,884,981 , GRCh37.p13 chr4: 122,805,723-122,806,136	TRPC3
nsv6739749	copy number variation	1	nstd229	human		GRCh38 chr4: 121,865,101-121,878,000 , GRCh37.p13 chr4: 122,786,256-122,799,155	TRPC3, BBS7
nsv6739735	copy number variation	1	nstd229	human		GRCh38 chr4: 121,745,676-122,710,918 , GRCh37.p13 chr4: 122,666,831-123,632,073	CCNA2, TRPC3, 13 more genes
nsv6570561	inversion	1	nstd223	human		GRCh38 chr4: 117,041,188-125,064,052 , GRCh37.p13 chr4: 117,962,344-125,985,207	MYOZ2, NT5C3AP1, 109 more genes
nsv6394900	copy number variation	1	nstd223	human		GRCh38 chr4: 121,906,129-121,906,813 , GRCh37.p13 chr4: 122,827,284-122,827,968	TRPC3
nsv6393104	copy number variation	1	nstd223	human		GRCh38 chr4: 121,903,873-121,904,358 , GRCh37.p13 chr4: 122,825,028-122,825,513	TRPC3
nsv6388914	copy number variation	1	nstd223	human		GRCh38 chr4: 121,932,001-121,933,300 , GRCh37.p13 chr4: 122,853,156-122,854,455	TRPC3
nsv6388560	copy number variation	1	nstd223	human		GRCh38 chr4: 121,914,854-121,924,289 , GRCh37.p13 chr4: 122,836,009-122,845,444	TRPC3

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Number of Variants: 20

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Has Clinical Interpretation

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Items: 1 to 20 of 281

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Number of Variants: 20

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