e2f3[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3888567	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 20,460,699-20,864,269 , GRCh38.p12 chr6: 20,460,468-20,864,038	E2F3, RPL36AP25, 2 more genes
nsv4675975	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 20,488,753-20,882,544 , GRCh38.p12 chr6: 20,488,522-20,882,313	E2F3, LOC105374968, 2 more genes
nsv6636333	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 12,005,630-22,849,647 , GRCh38.p12 chr6: 12,005,397-22,849,418	E2F3, SOX4, 136 more genes
nsv3875604	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 13,693,852-24,225,515 , GRCh38.p12 chr6: 13,693,620-24,225,287	E2F3, KIF13A, 124 more genes
nsv4456299	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 13,910,125-22,000,204 , GRCh38.p12 chr6: 13,909,894-21,999,975	E2F3, LOC101928354, 101 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	E2F3, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	E2F3, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	E2F3, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	E2F3, ITPR3, 2905 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	E2F3, TRR-ACG1-2, 1385 more genes
nsv3920564	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946	E2F3, PRELID1P2, 785 more genes
nsv3888615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 168,775-24,023,234 , GRCh38.p12 chr6: 168,775-24,023,006	E2F3, LOC107986557, 349 more genes
nsv3872568	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 168,775-24,023,234 , GRCh38.p12 chr6: 168,775-24,023,006	E2F3, TXNDC5, 349 more genes
nsv4456780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393	E2F3, LOC105374960, 342 more genes
nsv3886069	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 156,974-21,955,964 , GRCh38.p12 chr6: 156,974-21,955,733	E2F3, FOXCUT, 331 more genes
nsv7093363	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769	E2F3, LOC101928354, 321 more genes

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