e2f7[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3892030	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 69,608,090-89,629,345 , GRCh38.p12 chr12: 69,214,310-89,235,568	E2F7, LOC101928002, 197 more genes
nsv3922777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 73,879,477-93,189,581 , NCBI36 chr12: 72,165,744-91,713,712 , GRCh38 chr12: 73,485,697-92,795,805	E2F7, RN7SL734P, 195 more genes
nsv3924329	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 70,731,264-82,154,924 , GRCh38 chr12: 70,337,484-81,761,145 , NCBI36 chr12: 69,017,531-80,679,055	E2F7, NAV3, 118 more genes
nsv3918758	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 75,683,698-80,195,649 , NCBI36 chr12: 74,363,745-79,113,560 , GRCh37 chr12: 76,077,478-80,589,429	E2F7, YWHAQP7, 48 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	E2F7, 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	E2F7, 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	E2F7, 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	E2F7, 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	E2F7, OR5BT1P, 2441 more genes
nsv3924183	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr12: 75,484,784-80,938,999 , GRCh37 chr12: 76,960,653-82,414,868 , GRCh38 chr12: 76,566,873-82,021,089	E2F7, CSRP2, 52 more genes
nsv3904117	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 77,266,211-77,964,428 , GRCh38.p12 chr12: 76,872,431-77,570,648	E2F7, LOC727803, 4 more genes

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