col4a2[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
nsv6137692	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr13: 111,145,433-111,145,496 , GRCh38 chr13: 110,493,086-110,493,149	COL4A2
nsv3905048	copy number variation	1	nstd102	human	Benign	GRCh37 chr13: 110,959,350-110,961,114 , GRCh38.p12 chr13: 110,307,003-110,308,767	COL4A2, COL4A1
nsv3903901	copy number variation	1	nstd102	human	Benign	GRCh37 chr13: 110,959,529-110,961,114 , GRCh38.p12 chr13: 110,307,182-110,308,767	COL4A2, COL4A1
nsv3897914	copy number variation	1	nstd102	human	Benign	GRCh37 chr13: 110,959,350-110,960,146 , GRCh38.p12 chr13: 110,307,003-110,307,799	COL4A2, COL4A1
nsv6309333	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 111,098,156-111,111,301 , GRCh38.p12 chr13: 110,445,809-110,458,954	COL4A2, COL4A2-AS2
nsv4683614	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 110,802,710-110,959,374 , GRCh38.p12 chr13: 110,150,363-110,307,027	COL4A2, COL4A1
nsv5980390	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 110,802,791-110,959,290 , GRCh38.p12 chr13: 110,150,444-110,306,943	COL4A2, COL4A1
nsv7093989	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 110,822,874-110,960,490 , GRCh38.p12 chr13: 110,170,527-110,308,143	COL4A2, COL4A1
nsv4683960	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 110,959,271-110,959,394 , GRCh38.p12 chr13: 110,306,924-110,307,047	COL4A2, COL4A1
nsv3899879	copy number variation	1	nstd102	human	Benign	GRCh37 chr13: 110,848,498-111,132,556 , GRCh38.p12 chr13: 110,196,151-110,480,209	COL4A2, MIR8073, 2 more genes
nsv4729179	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 110,771,847-111,020,926 , GRCh38.p12 chr13: 110,119,500-110,368,579	COL4A2, LOC101927712, 3 more genes
nsv4681417	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr13: 111,102,026-111,176,544 , GRCh38.p12 chr13: 110,449,679-110,524,197	COL4A2, COL4A2-AS2, 2 more genes
nsv6309433	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 110,802,675-111,358,440 , GRCh38.p12 chr13: 110,150,328-110,706,093	COL4A2, COL4A1, 6 more genes
nsv3910270	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,445,862-114,327,173 , NCBI36 chr13: 10,098,739-114,110,750 , GRCh37 chr13: 19,020,001-115,085,141	COL4A2, RNU6-71P, 1332 more genes
nsv3924528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908	COL4A2, LOC105370271, 925 more genes
nsv4675850	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258	COL4A2, TEX30, 680 more genes
nsv6314171	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 79,370,012-115,107,733 , GRCh38.p12 chr13: 78,795,877-114,342,258	COL4A2, MIR4705, 430 more genes
nsv3920102	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 86,788,927-114,340,331 , GRCh37 chr13: 87,441,182-115,085,141 , NCBI36 chr13: 86,239,183-114,123,908	COL4A2, LOC107984609, 369 more genes
nsv3903376	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 88,073,140-115,107,733 , GRCh38.p12 chr13: 87,420,885-114,342,258	COL4A2, ZIC2, 364 more genes
nsv3896487	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 89,796,110-115,083,342 , GRCh38.p12 chr13: 89,143,856-114,317,867	COL4A2, TMTC4, 347 more genes

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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 127

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Number of Variants: 20

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