dbVar for Gene (Select 112577516) - 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
nsv5980446	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718	LINC02641, CFAP46, 194 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
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
nsv4675857	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 123,232,922-124,638,514 , GRCh38.p12 chr10: 121,473,408-122,878,998	LOC105378525, HTRA1, 20 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
nsv4208989	copy number variation	1	nstd166	human		GRCh37.p13 chr10: 123,721,898-126,209,916 , GRCh38.p12 chr10: 121,962,383-124,521,347	, CHST15, 44 more genes
nsv4200182	copy number variation	1	nstd166	human		GRCh37.p13 chr10: 124,422,538-124,478,190 , GRCh38.p12 chr10: 122,663,022-122,718,674	C10orf120, SPADH
nsv3956744	insertion	1	nstd168	human		GRCh38 chr10: 122,662,585-122,711,584 , GRCh37.p13 chr10: 124,422,101-124,471,100	C10orf120, SPADH
nsv3955592	copy number variation	1	nstd168	human		GRCh38 chr10: 122,656,190-122,683,831 , GRCh37.p13 chr10: 124,415,706-124,443,347	SPADH
nsv3924720	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 119,707,856-133,613,639 , GRCh37 chr10: 121,467,368-135,427,143 , NCBI36 chr10: 121,457,358-135,277,133	OR6L2P, RPL19P16, 208 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
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
nsv3922109	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 122,143,176-124,358,013 , NCBI36 chr10: 123,892,681-126,036,572 , GRCh37 chr10: 123,902,691-126,046,582	DMBT1L1, RPS26P39, 36 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
nsv3921792	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 123,338,496-135,284,168 , GRCh37 chr10: 123,348,506-135,434,178 , GRCh38 chr10: 121,588,992-133,620,674	LINC02641, FAM24B-CUZD1, 185 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

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Number of Variants: 20

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Organism

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Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 113

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Number of Variants: 20

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