dbVar for Gene (Select 2834) - 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
nsv6112765	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815	STK32C, LOC105378542, 266 more genes
nsv5974801	inversion	1	nstd209	human		GRCh38 chr10: 116,446,135-119,236,441 , GRCh37.p13 chr10: 118,205,647-120,995,953	EMX2, PRLHR, 48 more genes
nsv5672603	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 119,302,758-124,813,305 , GRCh38.p12 chr10: 117,543,247-123,053,789	ACADSB, DMBT1, 84 more genes
nsv5500799	copy number variation	1	nstd206	human		GRCh38 chr10: 118,346,368-118,602,368 , GRCh37.p13 chr10: 120,105,880-120,361,880	PRLHR, SLC25A18P1, 2 more genes
nsv4977168	copy number variation	1	nstd200	human		GRCh38 chr10: 118,590,581-118,591,845 , GRCh37.p13 chr10: 120,350,093-120,351,357	PRLHR
nsv4848436	copy number variation	1	nstd200	human		GRCh37 chr10: 120,350,093-120,351,357 , GRCh38.p12 chr10: 118,590,581-118,591,845	PRLHR
nsv4675991	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639	STK32C, LOC105378542, 237 more genes
nsv4456626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639	LOC105378521, ZRANB1, 317 more genes
nsv4349508	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 117,024,753-124,942,806 , GRCh38.p12 chr10: 115,265,276-123,183,290	PRLHR, LOC105378513, 121 more genes
nsv4348764	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591	LOC105378492, VENTX, 373 more genes
nsv4342336	sequence alteration	1	nstd166	human		GRCh37.p13 chr10: 118,638,442-121,163,255 , GRCh38.p12 chr10: 116,878,931-119,403,743	EIF3A, VAX1, 38 more genes
nsv3923859	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 113,062,847-135,284,168 , GRCh37 chr10: 113,072,857-135,434,178 , GRCh38 chr10: 111,313,099-133,620,674	AS-PTPRE, SFXN4, 330 more genes
nsv3923769	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291	LOC105378493, LINC02627, 477 more genes
nsv3923545	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 118,330,136-118,685,873 , NCBI36 chr10: 120,079,638-120,435,375 , GRCh37 chr10: 120,089,648-120,445,385	PRLHR, FAM204A, 5 more genes
nsv3922274	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr10: 103,274,160-135,374,737 , GRCh37.p13 chr10: 103,284,170-135,524,747 , GRCh38.p12 chr10: 101,524,413-133,787,422	DPCD, LOC105378467, 504 more genes
nsv3921919	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 100,600,492-133,622,588 , GRCh37 chr10: 102,360,249-135,436,092 , NCBI36 chr10: 102,350,239-135,286,082	MIR4295, BORCS7, 508 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	EIF2S2P3, CYP17A1-AS1, 895 more genes
nsv3919820	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 107,191,100-118,761,489 , GRCh37 chr10: 108,950,858-120,521,001 , NCBI36 chr10: 108,940,848-120,510,991	CCDC186, RN7SKP288, 147 more genes
nsv3919433	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr10: 119,668,832-121,236,830 , GRCh37.p13 chr10: 119,678,842-121,246,840 , GRCh38.p12 chr10: 117,919,331-119,487,328	EIF3A, RN7SL749P, 23 more genes
nsv3914619	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 111,418,518-126,431,209 , GRCh37.p13 chr10: 111,428,528-126,441,219 , GRCh38.p12 chr10: 109,668,770-124,752,650	LOC103344931, LINC02626, 225 more genes

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Has Clinical Interpretation

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Items: 1 to 20 of 85

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Number of Variants: 20

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