tnfrsf11b[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5674051	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 119,936,613-119,964,060 , GRCh38.p12 chr8: 118,924,374-118,951,821	TNFRSF11B, COLEC10
nsv6315139	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 118,690,580-118,950,848 , GRCh37.p13 chr8: 119,702,819-119,963,087	TNFRSF11B, COLEC10, 3 more genes
nsv3886360	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 119,932,595-120,030,098 , GRCh38 chr8: 118,920,356-119,017,859	TNFRSF11B, RNU6-12P, 2 more genes
nsv6291164	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 119,933,300-120,031,575 , GRCh38.p12 chr8: 118,921,061-119,019,336	TNFRSF11B, LOC100286746, 2 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	RNU6-71P, LINC00676, 1332 more genes
nsv3924528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908	LOC105370271, OR7E33P, 925 more genes
nsv4675850	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258	TEX30, LOC101927712, 680 more genes
nsv3907697	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 53,551,300-109,850,651 , GRCh38.p12 chr13: 52,977,165-109,198,303	GPC5, SNORD31B, 565 more genes
nsv3898603	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 42,457,841-91,796,698 , GRCh38.p12 chr13: 41,883,705-91,144,444	RNY4P30, LOC107987191, 575 more genes
nsv3918812	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 44,967,523-92,738,168 , NCBI36 chr13: 44,439,658-92,188,422 , GRCh37 chr13: 45,541,658-93,390,421	SRSF1P1, LOC105370213, 541 more genes
nsv6314117	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618	RBM26, RNY4P31, 591 more genes
nsv3913649	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 41,143,820-85,137,552 , GRCh37 chr13: 41,717,956-85,711,687 , NCBI36 chr13: 40,615,956-84,609,688	RPL21P108, LINC00330, 539 more genes
nsv3882264	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 46,968,080-87,381,985 , GRCh37.p13 chr13: 47,542,215-88,034,240	ARL11, RPL18P10, 428 more genes
nsv4675995	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 51,512,603-91,631,111 , GRCh38.p12 chr13: 50,938,467-90,978,857	RNU7-88P, LINC00564, 396 more genes
nsv3895373	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 57,058,434-94,684,615 , GRCh38.p12 chr13: 56,484,300-94,032,361	LINC00383, LOC105370250, 359 more genes
nsv3915859	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 47,117,587-84,300,935 , GRCh37 chr13: 47,691,722-84,875,070 , NCBI36 chr13: 46,589,723-83,773,071	LOC105370231, RNY1P6, 406 more genes
nsv6291752	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 59,574,760-89,410,027 , GRCh38.p12 chr13: 59,000,626-88,757,773	GYG1P2, LOC102723968, 284 more genes
nsv3913682	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 61,110,478-85,127,323 , NCBI36 chr13: 60,008,479-84,025,324 , GRCh38 chr13: 60,536,344-84,553,188	LOC105370251, MIR548X2, 236 more genes
nsv3902290	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 61,686,543-83,302,092 , GRCh38.p12 chr13: 61,112,409-82,727,957	LOC107987191, RNU4-10P, 216 more genes
nsv3918305	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 66,895,130-88,507,684 , GRCh38 chr13: 66,320,998-87,855,429 , NCBI36 chr13: 65,793,131-87,305,685	LINC00397, LINC00446, 208 more genes

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

Send to:

Search results

Items: 1 to 20 of 124

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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 124

Page of 7

Number of Variants: 20

Page of 7

Supplemental Content

Find related data

Search details

Recent activity