b3glct[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
nsv7093995	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 31,835,063-31,835,239 , GRCh38.p12 chr13: 31,260,926-31,261,102	B3GLCT
nsv4681195	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 31,774,202-31,860,976 , GRCh38.p12 chr13: 31,200,065-31,286,839	B3GLCT
nsv6309676	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 31,774,222-31,860,976 , GRCh38.p12 chr13: 31,200,085-31,286,839	B3GLCT
nsv3917076	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr13: 30,627,646-30,756,813 , GRCh38 chr13: 31,155,509-31,284,676 , GRCh37 chr13: 31,729,646-31,858,813	B3GLCT, HSPH1, 1 more genes
nsv3898732	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr13: 31,729,646-31,835,742 , GRCh38.p12 chr13: 31,155,509-31,261,605	B3GLCT, LOC105370148, 1 more genes
nsv3922568	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr13: 30,796,523-31,463,368 , GRCh37.p13 chr13: 31,898,523-32,565,368 , GRCh38.p12 chr13: 31,324,386-31,991,231	B3GLCT, RXFP2, 3 more genes
nsv3898113	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 31,846,981-32,194,074 , GRCh38.p12 chr13: 31,272,844-31,619,937	B3GLCT, LOC105370150, 1 more genes
nsv3910270	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,445,862-114,327,173 , NCBI36 chr13: 10,098,739-114,110,750 , GRCh37 chr13: 19,020,001-115,085,141	B3GLCT, RNU6-71P, 1332 more genes
nsv3915679	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 31,271,865-70,046,105 , GRCh38 chr13: 30,697,728-69,471,973 , NCBI36 chr13: 30,169,865-68,944,106	B3GLCT, CCDC70, 524 more genes
nsv3921404	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 31,592,297-49,065,340 , GRCh38 chr13: 31,018,160-48,491,204 , NCBI36 chr13: 30,490,297-47,963,341	B3GLCT, MIR8079, 280 more genes
nsv3924246	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 29,785,946-38,739,818 , GRCh37 chr13: 30,887,946-39,841,818 , GRCh38 chr13: 30,313,809-39,267,681	B3GLCT, LINC01048, 117 more genes
nsv3920559	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 29,647,457-37,130,151 , NCBI36 chr13: 28,545,457-36,028,151 , GRCh38 chr13: 29,073,320-36,556,014	B3GLCT, LINC02343, 92 more genes
nsv6112810	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 28,925,153-34,061,696 , GRCh38.p12 chr13: 28,351,016-33,487,559	B3GLCT, MTUS2, 70 more genes
nsv3916701	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 31,164,047-34,428,736 , NCBI36 chr13: 30,636,184-33,900,873 , GRCh37 chr13: 31,738,184-35,002,873	B3GLCT, RNY1P4, 32 more genes
nsv3923402	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 30,228,271-33,432,383 , GRCh38 chr13: 29,654,134-32,858,245 , NCBI36 chr13: 29,126,271-32,330,383	B3GLCT, RXFP2, 53 more genes
nsv3894881	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 31,682,663-33,765,790 , GRCh38.p12 chr13: 31,108,526-33,191,653	B3GLCT, IFIT1P1, 24 more genes
nsv6315495	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403	B3GLCT, RNU6-80P, 1334 more genes
nsv6289999	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403	B3GLCT, LINC00363, 1334 more genes
nsv3897246	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,031,237-115,107,157 , GRCh38.p12 chr13: 18,457,097-114,341,682	B3GLCT, NT5CP3, 1334 more genes
nsv3924676	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862	B3GLCT, GRTP1, 1334 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 47

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Number of Variants: 20

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Supplemental Content

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Search details

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