dbVar for Gene (Select 101927944) - 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
nsv5373317	translocation	1	nstd200	human		GRCh38 chr10: 124,715,877-124,715,877 , GRCh38 chr10: 124,712,997-124,712,997 , GRCh37.p13 chr10: 126,401,566-126,401,566 , GRCh37.p13 chr10: 126,404,446-126,404,446	FAM53B-AS1, FAM53B
nsv4977385	copy number variation	1	nstd200	human		GRCh38 chr10: 124,712,969-124,714,208 , GRCh37.p13 chr10: 126,401,538-126,402,777	FAM53B-AS1, FAM53B
nsv4846101	copy number variation	1	nstd200	human		GRCh37 chr10: 126,402,231-126,403,210 , GRCh38.p12 chr10: 124,713,662-124,714,641	FAM53B-AS1, FAM53B
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
nsv4618033	copy number variation	1	nstd183	human		GRCh37 chr10: 126,292,159-126,420,498 , GRCh38.p12 chr10: 124,603,590-124,731,929	, FAM53B, 2 more genes
nsv4456733	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 124,988,334-135,427,143 , GRCh38.p12 chr10: 123,228,818-133,613,639	FAM53B-AS1, LOC105378544, 153 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
nsv4383148	copy number variation	1	nstd173	human		GRCh37 chr10: 126,401,796-126,456,614 , GRCh38.p12 chr10: 124,713,227-124,768,045	FAM53B, FAM53B-AS1, 1 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
nsv4202914	copy number variation	1	nstd166	human		GRCh37.p13 chr10: 126,401,566-126,402,750 , GRCh38.p12 chr10: 124,712,997-124,714,181	FAM53B, FAM53B-AS1
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
nsv3922547	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 124,576,249-128,409,507 , GRCh37 chr10: 124,586,259-128,419,517 , GRCh38 chr10: 122,826,743-126,730,948	FAM53B, LOC107984184, 70 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
nsv3922119	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 125,792,404-129,167,091 , NCBI36 chr10: 125,782,394-129,057,081 , GRCh38 chr10: 124,032,888-127,368,827	LINC00601, LOC105378545, 53 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

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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

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Study Type

Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 147

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Number of Variants: 20

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