ago2[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
nsv3901319	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 141,644,176-141,646,299 , GRCh38.p12 chr8: 140,634,077-140,636,200	AGO2
nsv3902463	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 141,646,069-141,646,248 , GRCh38.p12 chr8: 140,635,970-140,636,149	AGO2
nsv3906947	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 141,621,038-141,690,979 , GRCh38.p12 chr8: 140,610,939-140,680,880	AGO2, LOC107986982, 1 more genes
nsv6637760	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 141,352,715-141,656,635 , GRCh38.p12 chr8: 140,342,616-140,646,536	AGO2, LOC107986982, 3 more genes
nsv3909966	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr8: 141,516,995-141,651,401 , GRCh37.p13 chr8: 141,447,813-141,582,219 , GRCh38.p12 chr8: 140,437,714-140,572,120	AGO2, LOC105375782, 2 more genes
nsv4457242	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 141,617,375-141,747,946 , GRCh38.p12 chr8: 140,607,276-140,737,847	AGO2, PTK2, 2 more genes
nsv4455527	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 141,431,936-141,542,147 , GRCh38.p12 chr8: 140,421,837-140,532,048	AGO2, LOC105375782, 2 more genes
nsv3891604	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 141,447,774-141,542,712 , GRCh38.p12 chr8: 140,437,675-140,532,613	AGO2, LOC105375782, 2 more genes
nsv4674996	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 126,892,814-143,750,028 , GRCh38.p12 chr8: 125,880,570-142,668,610	AGO2, POU5F1B, 158 more genes
nsv3915490	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 127,707,788-144,459,935 , GRCh37.p13 chr8: 127,638,606-144,388,560 , GRCh38.p12 chr8: 126,626,361-143,306,390	AGO2, LOC107986906, 179 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	AGO2, 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	AGO2, 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	AGO2, 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	AGO2, 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	AGO2, 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	AGO2, 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	AGO2, 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	AGO2, 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	AGO2, 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	AGO2, MIR4662B, 2104 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 64

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Number of Variants: 20

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