nipal3[All Fields] AND 1[has_clinical] - dbVar - NCBI

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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
nsv3873478	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 24,798,383-24,809,462 , GRCh38.p12 chr1: 24,471,893-24,482,972	NIPAL3
nsv3888534	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 24,798,383-24,807,014 , GRCh38.p12 chr1: 24,471,893-24,480,524	NIPAL3
nsv6315431	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 24,531,639-24,749,706 , GRCh38.p12 chr1: 24,205,149-24,423,216	NIPAL3, STPG1, 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	NIPAL3, 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	NIPAL3, 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	NIPAL3, 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	NIPAL3, 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	NIPAL3, LINC01776, 1853 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	NIPAL3, GRHL3, 16 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	NIPAL3, LOC105376864, 13 more genes

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