hmgn2[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	HMGN2, 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	HMGN2, 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	HMGN2, RNU1-153P, 4887 more genes
nsv3901163	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 24,707,696-41,886,350 , GRCh38 chr1: 24,381,206-41,401,517 , NCBI36 chr1: 24,580,283-41,658,937	HMGN2, TMEM222, 453 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	HMGN2, LINC01776, 1853 more genes
nsv7095609	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 25,870,190-27,278,871 , GRCh38.p12 chr1: 25,543,699-26,952,380	HMGN2, RPL34P4, 53 more genes
nsv6290421	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 26,246,213-27,044,118 , GRCh38.p12 chr1: 25,919,722-26,717,627	HMGN2, C1orf232, 32 more genes
nsv4453629	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 26,603,699-26,903,828 , GRCh38.p12 chr1: 26,277,208-26,577,337	HMGN2, CEP85, 13 more genes

dbVar