hnrnpr[All Fields] AND 1[has_clinical] - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	HNRNPR, 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	HNRNPR, 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	HNRNPR, 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	HNRNPR, 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	HNRNPR, RPL29P6, 156 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	HNRNPR, 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	HNRNPR, ALPL, 174 more genes

dbVar