dbVar for Gene (Select 106481383) - 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
nsv4676104	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963	LLGL2, TSEN54, 165 more genes
nsv4457646	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062	LOC107985089, ARSG, 448 more genes
nsv4262229	copy number variation	1	nstd166	human		GRCh37.p13 chr17: 76,649,383-77,059,909 , GRCh38.p12 chr17: 78,653,301-79,063,827	, CEP295NL, 9 more genes
nsv3920061	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr17: 73,733,032-75,688,373 , GRCh37 chr17: 76,221,437-78,073,778 , GRCh38 chr17: 78,225,356-80,099,979	BIRC5, GAA, 38 more genes
nsv3919635	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 76,088,317-81,044,553 , NCBI36 chr17: 73,599,912-78,637,842 , GRCh38 chr17: 78,092,236-83,086,677	LINC03048, MIR3186, 154 more genes
nsv3919156	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717	CD300A, RNF213, 359 more genes
nsv3917730	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr17: 78,484,862-79,436,025 , NCBI36 chr17: 73,992,539-74,943,702 , GRCh37 chr17: 76,480,944-77,432,107	C1QTNF1, TIMP2, 15 more genes
nsv3917654	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 64,716,815-78,637,842 , GRCh37 chr17: 67,205,220-81,044,553 , GRCh38 chr17: 69,209,079-83,086,677	LOC101928447, GRB2, 368 more genes
nsv3914783	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577	LOC105371922, GJD3, 1855 more genes
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	PRPSAP1, CACNG1, 1350 more genes
nsv3909523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062	RPL38, RNF157-AS1, 428 more genes
nsv3909511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846	FOXK2, SOCS3-DT, 958 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	SMURF2, LOC112268199, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	MIR21, LOC105371899, 2366 more genes
nsv3906075	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 67,002,415-81,041,938 , GRCh38.p12 chr17: 69,006,274-83,084,062	CEP131, RPTOR, 374 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	MIR3185, YWHAEP6, 2366 more genes
nsv3903515	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 76,676,371-77,287,185 , GRCh38.p12 chr17: 78,680,289-79,291,103	CANT1, RPL9P29, 10 more genes
nsv3903359	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 76,395,581-76,703,281 , GRCh38.p12 chr17: 78,399,500-78,707,199	PGS1, LOC100419624, 6 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	P4HB, LOC105371808, 2366 more genes
nsv3897835	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 73,951,701-81,041,938 , GRCh38.p12 chr17: 75,955,620-83,084,062	ARHGDIA, CCDC137, 230 more genes

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Number of Variants: 20

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Organism

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Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 127

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Number of Variants: 20

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