il27ra[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3898633	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr19: 14,141,495-14,142,319 , GRCh38.p12 chr19: 14,030,683-14,031,507	IL27RA, RLN3
nsv3907342	copy number variation	1	nstd102	human	conflicting data from submitters	GRCh37 chr19: 14,139,111-14,150,649 , GRCh38.p12 chr19: 14,028,299-14,039,837	IL27RA, RLN3
nsv3891771	copy number variation	1	nstd102	human	conflicting data from submitters	GRCh37 chr19: 14,139,111-14,162,382 , GRCh38.p12 chr19: 14,028,299-14,051,570	IL27RA, RLN3, 1 more genes
nsv3924466	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,496,978-14,126,833 , GRCh38 chr19: 11,525,163-14,155,021 , GRCh37 chr19: 11,635,978-14,265,833	IL27RA, JUNB, 135 more genes
nsv3908579	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 14,124,666-16,431,349 , GRCh38.p12 chr19: 14,013,854-16,320,538	IL27RA, TMEM167AP2, 99 more genes
nsv3912480	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 12,580,427-14,742,673 , GRCh37 chr19: 12,691,241-14,853,485 , NCBI36 chr19: 12,552,241-14,714,485	IL27RA, GET3, 100 more genes
nsv3907864	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 12,574,343-14,726,197 , GRCh38.p12 chr19: 12,463,529-14,615,385	IL27RA, WDR83, 105 more genes
nsv3910509	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 13,505,739-15,342,900 , GRCh37 chr19: 13,644,739-15,481,900 , GRCh38 chr19: 13,533,925-15,371,089	IL27RA, DDX39A, 76 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	IL27RA, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	IL27RA, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	IL27RA, LENG8, 2408 more genes
nsv3913730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354	IL27RA, BCKDHA, 1102 more genes
nsv3922457	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 14,085,489-28,330,584 , GRCh38 chr19: 13,974,677-27,839,676 , NCBI36 chr19: 13,946,489-33,022,424	IL27RA, REX1BD, 416 more genes
nsv3898900	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 9,678,768-14,853,426 , GRCh38.p12 chr19: 9,568,092-14,742,614	IL27RA, FBXL12, 253 more genes
nsv3923415	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 10,286,934-14,020,806 , GRCh37 chr19: 10,425,934-14,159,806 , GRCh38 chr19: 10,315,258-14,048,994	IL27RA, MAN2B1, 182 more genes
nsv3915094	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 12,132,052-14,751,798 , NCBI36 chr19: 12,103,867-14,723,610 , GRCh37 chr19: 12,242,867-14,862,610	IL27RA, RN7SL619P, 123 more genes
nsv3891875	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 13,592,592-14,717,528 , GRCh38.p12 chr19: 13,481,778-14,606,716	IL27RA, CACNA1A, 48 more genes
nsv3913955	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 13,644,739-14,369,645 , GRCh38 chr19: 13,533,925-14,258,833 , NCBI36 chr19: 13,505,739-14,230,645	IL27RA, YJU2B, 30 more genes
nsv3899944	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 11,608,072-14,543,046 , GRCh38.p12 chr19: 11,497,257-14,432,234	IL27RA, RNA5SP465, 145 more genes

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