angpt4[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
nsv3906049	copy number variation	1	nstd102	human	Benign	GRCh37 chr20: 837,800-854,940 , GRCh38.p12 chr20: 857,157-874,297	ANGPT4
nsv4676270	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,568-2,269,777 , GRCh38.p12 chr20: 80,927-2,289,131	ANGPT4, LOC100289473, 60 more genes
nsv3917810	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 121,781-2,290,194 , GRCh37 chr20: 102,422-2,270,840 , NCBI36 chr20: 50,422-2,218,840	ANGPT4, RAD21L1, 59 more genes
nsv1398608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 71,023-2,129,746 , GRCh38.p12 chr20: 90,382-2,149,100	ANGPT4, SIRPB3P, 58 more genes
nsv3899121	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 121,521-2,073,612 , GRCh38.p12 chr20: 140,880-2,092,966	ANGPT4, RN7SL561P, 56 more genes
nsv3914701	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 70,580-1,919,864 , NCBI36 chr20: 18,580-1,867,864 , GRCh38 chr20: 89,939-1,939,218	ANGPT4, MIR6869, 54 more genes
nsv3916212	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-1,781,123 , GRCh37 chr20: 70,580-1,833,123 , GRCh38 chr20: 89,939-1,852,477	ANGPT4, NRSN2-AS1, 52 more genes
nsv3907056	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,568-1,823,540 , GRCh38.p12 chr20: 80,927-1,842,894	ANGPT4, ACTG1P3, 52 more genes
nsv3923563	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-1,699,213 , GRCh37 chr20: 70,580-1,751,213 , GRCh38 chr20: 89,939-1,770,567	ANGPT4, LOC101929937, 50 more genes
nsv3924759	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-1,422,759 , GRCh38 chr20: 89,939-1,494,113 , GRCh37 chr20: 70,580-1,474,759	ANGPT4, DEFB127, 39 more genes
nsv3915146	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-1,288,754 , GRCh38 chr20: 89,939-1,360,110 , GRCh37 chr20: 70,580-1,340,754	ANGPT4, TMEM74B, 34 more genes
nsv4676288	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,568-1,305,971 , GRCh38.p12 chr20: 80,927-1,325,327	ANGPT4, TBC1D20, 34 more genes
nsv3914263	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 80,093-1,246,766 , NCBI36 chr20: 8,734-1,175,410 , GRCh37 chr20: 60,734-1,227,410	ANGPT4, TBC1D20, 30 more genes
nsv5381806	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 67,778-974,841 , GRCh38.p12 chr20: 87,137-994,198	ANGPT4, DEFB132, 24 more genes
nsv3914223	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 89,939-975,656 , GRCh37 chr20: 70,580-956,299 , NCBI36 chr20: 18,580-904,299	ANGPT4, DEFB125, 24 more genes
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	ANGPT4, TGIF2-RAB5IF, 1314 more genes
nsv3905072	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435	ANGPT4, LRRN4, 1313 more genes
nsv3895314	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202	ANGPT4, PKIG, 1311 more genes
nsv3896520	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110	ANGPT4, COMMD7, 1311 more genes
nsv3920218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118	ANGPT4, MIR3646, 1310 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 53

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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