opn5[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 10

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3923721	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 45,681,671-54,212,044 , GRCh37 chr6: 45,649,408-54,076,842 , NCBI36 chr6: 45,757,386-54,184,801	OPN5, PAQR8, 131 more genes
nsv3884243	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 43,636,308-50,947,320 , GRCh38.p12 chr6: 43,668,571-50,979,607	OPN5, GLYATL3, 105 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	OPN5, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	OPN5, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	OPN5, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	OPN5, ITPR3, 2905 more genes
nsv4350067	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650	OPN5, HLA-DPB2, 1001 more genes
nsv3913758	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr6: 47,267,474-51,400,063 , GRCh37 chr6: 47,159,515-51,292,104 , GRCh38 chr6: 47,191,779-51,427,306	OPN5, CRISP1, 46 more genes
nsv6314749	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313	OPN5, ACTG1P9, 245 more genes
nsv3919465	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr6: 45,061,475-48,062,533 , GRCh37 chr6: 44,953,497-47,954,574 , GRCh38 chr6: 44,985,760-47,986,838	OPN5, ACTG1P9, 40 more genes

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