stn1[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
nsv4456807	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 105,640,552-105,676,813 , GRCh38.p12 chr10: 103,880,794-103,917,055	STN1
nsv7093857	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 105,648,810-105,677,352 , GRCh38.p12 chr10: 103,889,052-103,917,594	STN1
nsv6308899	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 105,642,442-105,677,352 , GRCh38.p12 chr10: 103,882,684-103,917,594	STN1
nsv6314221	insertion	1	nstd102	human	Uncertain significance	GRCh38 chr10: 103,900,166-103,900,166 , GRCh37 chr10: 105,659,924-105,659,924	STN1
nsv3905399	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 105,675,946-105,791,929 , GRCh38.p12 chr10: 103,916,188-104,032,171	STN1, SLK, 3 more genes
nsv3880331	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 48,707,080-48,763,742 , GRCh38.p12 chr2: 48,479,941-48,536,603	STON1-GTF2A1L, PPP1R21, 2 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	STN1, RNU7-12P, 1876 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	CYP1B1-AS1, LOC107985771, 1649 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	STN1, EIF2S2P3, 895 more genes
nsv3905499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 104,030,479-115,410,590 , GRCh38.p12 chr10: 102,270,722-113,650,831	STN1, RPS15AP30, 156 more genes
nsv3916477	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 104,481,920-115,834,854 , GRCh37 chr10: 104,491,930-115,844,864 , GRCh38 chr10: 102,732,173-114,085,105	STN1, XPNPEP1, 147 more genes
nsv3875808	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 47,361,260-54,934,153 , GRCh38.p12 chr2: 47,134,121-54,707,016	FOXN2, EPCAM-DT, 85 more genes
nsv3898065	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 47,033,357-50,792,676 , NCBI36 chr2: 46,886,861-50,646,180 , GRCh38 chr2: 46,806,218-50,565,538	CALM2, NRXN1, 49 more genes
nsv3924696	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 102,243,341-103,929,730 , GRCh37 chr10: 104,003,098-105,689,488 , NCBI36 chr10: 103,993,088-105,679,478	STN1, MIR146B, 48 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	LOC112268439, RNA5SP116, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	IGKV2OR2-10, LOC105374848, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	RNU6-674P, KANSL3, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	MTND2P22, LOC112268410, 3724 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	STN1, LOC100419870, 2105 more genes
nsv3891157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558	STN1, AGAP14P, 2097 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 52

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Number of Variants: 20

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