e2f5[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3896604	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 86,021,909-86,099,942 , GRCh38.p12 chr8: 85,109,674-85,187,707	E2F5, LRRCC1, 2 more genes
nsv3891865	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 86,021,909-86,099,701 , GRCh38.p12 chr8: 85,109,674-85,187,466	E2F5, E2F5-DT, 2 more genes
nsv3902289	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 86,021,909-86,088,198 , GRCh38.p12 chr8: 85,109,674-85,175,963	E2F5, LOC105375933, 2 more genes
nsv3907448	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 86,021,913-86,088,198 , GRCh38.p12 chr8: 85,109,678-85,175,963	E2F5, E2F5-DT, 2 more genes
nsv4457138	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 86,114,785-86,214,050 , GRCh38.p12 chr8: 85,202,550-85,301,821	E2F5, LOC105375936, 2 more genes
nsv3911034	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 79,584,698-96,379,096 , NCBI36 chr8: 79,747,253-96,448,272 , GRCh38 chr8: 78,672,463-95,366,868	E2F5, LOC105375933, 233 more genes
nsv3914059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 78,677,666-92,851,513 , GRCh38 chr8: 77,765,431-91,839,285 , NCBI36 chr8: 78,840,221-92,920,689	E2F5, RN7SL107P, 176 more genes
nsv3922848	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 74,954,174-86,710,947 , GRCh37 chr8: 74,791,620-86,523,695 , GRCh38 chr8: 73,879,385-85,611,466	E2F5, MITA1, 139 more genes
nsv6315163	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 75,904,944-87,097,083 , GRCh38.p12 chr8: 74,992,709-86,084,854	E2F5, ZNF704, 137 more genes
nsv6313579	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 77,906,471-88,917,707 , GRCh38.p12 chr8: 76,994,235-87,905,479	E2F5, LOC105375915, 143 more genes
nsv3915173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636	E2F5, RN7SL474P, 2109 more genes
nsv3901821	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028	E2F5, TBC1D31, 2109 more genes
nsv4349554	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385	E2F5, LOC101929488, 2105 more genes
nsv3916777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575	E2F5, RPL5P22, 2105 more genes
nsv3898123	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385	E2F5, SPAG1, 2105 more genes
nsv3908608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028	E2F5, LINC01617, 2105 more genes
nsv3893757	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442	E2F5, LOC105375890, 2105 more genes
nsv3923310	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098	E2F5, LOC112268023, 2105 more genes
nsv3914307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,605-146,280,167 , GRCh38 chr8: 241,605-145,054,781 , NCBI36 chr8: 181,605-146,250,971	E2F5, LOC107986897, 2104 more genes
nsv3919282	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824	E2F5, MIR4662B, 2104 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 40

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Number of Variants: 20

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Supplemental Content

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Search details

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