il22ra1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 13

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3873229	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 24,382,298-24,448,084 , GRCh38.p12 chr1: 24,055,808-24,121,594	IL22RA1, MYOM3-AS1, 3 more genes
nsv6636837	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 24,409,165-24,492,808 , GRCh38.p12 chr1: 24,082,675-24,166,318	IL22RA1, LOC105376864, 3 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	IL22RA1, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	IL22RA1, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	IL22RA1, RNU1-153P, 4887 more genes
nsv4436181	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532	IL22RA1, LINC01776, 1853 more genes
nsv7095949	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371	IL22RA1, RPL29P6, 156 more genes
nsv4684226	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 24,394,811-25,148,686 , GRCh38.p12 chr1: 24,068,321-24,822,195	IL22RA1, GRHL3, 16 more genes
nsv6636627	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 24,111,388-24,686,443 , GRCh38.p12 chr1: 23,784,898-24,359,953	IL22RA1, MYOM3-AS1, 23 more genes
nsv6636637	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 24,363,507-24,875,537 , GRCh38.p12 chr1: 24,037,017-24,549,046	IL22RA1, LOC105376864, 13 more genes
nsv6636630	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 24,111,522-24,614,856 , GRCh38.p12 chr1: 23,785,032-24,288,366	IL22RA1, HMGCL, 20 more genes
nsv4436680	complex substitution	1	nstd102	human	Uncertain significance	GRCh38.p12 chr1: 973,858-24,379,779 , GRCh37 chr1: 909,238-24,706,269	IL22RA1, ALPL, 636 more genes
nsv4436486	complex substitution	1	nstd102	human	Uncertain significance	GRCh38.p12 chr1: 17,229,013-24,379,779 , GRCh37 chr1: 17,555,508-24,706,269	IL22RA1, ALPL, 174 more genes

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