stat2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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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
nsv7094148	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 56,739,910-56,740,759 , GRCh38.p12 chr12: 56,346,126-56,346,975	STAT2
nsv4450703	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 56,737,153-56,737,939 , GRCh38 chr12: 56,343,369-56,344,155	STAT2
nsv3876474	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr12: 56,343,369-56,356,591 , GRCh37 chr12: 56,737,153-56,750,375	STAT2, RNU7-40P
nsv3875525	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr12: 56,346,126-56,356,591 , GRCh37 chr12: 56,739,910-56,750,375	STAT2, RNU7-40P
nsv6309482	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 56,739,910-56,750,355 , GRCh38.p12 chr12: 56,346,126-56,356,571	STAT2, RNU7-40P
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	STAT2, RNA5SP369, 2454 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	STAT2, LOH12CR2, 2452 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	STAT2, RNU4ATAC16P, 2452 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	STAT2, BTG1P1, 2451 more genes
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	STAT2, OR5BT1P, 2441 more genes
nsv4675143	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 55,552,371-62,126,304 , GRCh38.p12 chr12: 55,158,587-61,732,523	STAT2, OR6C71P, 183 more genes
nsv6315199	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr12: 55,986,511-56,885,590 , GRCh37.p13 chr12: 56,380,295-57,279,374	STAT2, ERBB3, 47 more genes
nsv6313979	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 56,333,262-57,010,442 , GRCh38.p12 chr12: 55,939,478-56,616,658	STAT2, TRS-CGA4-1, 42 more genes

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