angpt2[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
nsv6636158	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 6,499,632-6,563,245 , GRCh37.p13 chr8: 6,357,153-6,420,766	ANGPT2, MCPH1
nsv7097666	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 6,357,353-6,357,470 , GRCh38.p12 chr8: 6,499,832-6,499,949	ANGPT2, MCPH1
nsv6312918	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 6,264,189-6,420,455 , GRCh38.p12 chr8: 6,406,668-6,562,934	ANGPT2, MCPH1, 2 more genes
nsv6312647	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 6,299,568-6,500,570 , GRCh38.p12 chr8: 6,442,047-6,643,049	ANGPT2, MCPH1, 3 more genes
nsv4455600	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 6,270,095-6,466,608 , GRCh38.p12 chr8: 6,412,574-6,609,087	ANGPT2, MCPH1, 1 more genes
nsv7097906	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 6,372,178-6,500,570 , GRCh38.p12 chr8: 6,514,657-6,643,049	ANGPT2, MIR8055, 2 more genes
nsv3901093	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 6,270,298-6,374,065 , GRCh38.p12 chr8: 6,412,777-6,516,544	ANGPT2, MCPH1, 1 more genes
nsv4685703	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 6,160,874-6,500,521 , GRCh38.p12 chr8: 6,303,353-6,643,000	ANGPT2, MCPH1, 4 more genes
nsv7097802	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 6,264,189-6,500,570 , GRCh38.p12 chr8: 6,406,668-6,643,049	ANGPT2, MCPH1, 4 more genes
nsv6315449	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940	ANGPT2, LOC101928016, 568 more genes
nsv3917350	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 2,292,235-27,361,796 , GRCh38 chr8: 2,475,295-27,504,279 , NCBI36 chr8: 2,121,457-27,417,713	ANGPT2, LINC03022, 472 more genes
nsv7148253	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417	ANGPT2, ENTPD4, 447 more genes
nsv6636968	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-18,936,715 , GRCh38.p12 chr8: 208,049-19,079,205	ANGPT2, ZNF705B, 357 more genes
nsv4455719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-14,214,722 , GRCh38.p12 chr8: 208,048-14,357,213	ANGPT2, MIR598, 312 more genes
nsv4685988	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 161,516-11,516,619 , GRCh38.p12 chr8: 211,516-11,659,110	ANGPT2, ZNF705B, 232 more genes
nsv7148131	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,501-11,142,629 , GRCh38.p12 chr8: 60,501-11,285,120	ANGPT2, XKR6, 224 more genes
nsv6634376	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-11,281,408 , GRCh38.p12 chr8: 208,048-11,423,899	ANGPT2, DLGAP2-AS1, 228 more genes
nsv6636940	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-10,965,627 , GRCh38.p12 chr8\|NW_018654717.1: 1-5,513,617 , GRCh38.p12 chr8: 208,049-11,108,117	ANGPT2, HSPD1P3, 270 more genes
nsv3902717	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-10,939,681 , GRCh38.p12 chr8: 208,048-11,082,171 , GRCh38.p12 chr8\|NW_018654717.1: 1-5,513,617	ANGPT2, LOC101929128, 270 more genes
nsv3921576	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,530-10,724,642 , GRCh38 chr8: 241,530-10,867,132 , NCBI36 chr8: 181,530-10,762,052	ANGPT2, SPAG11B, 213 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 124

Page of 7

Number of Variants: 20

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