cln5[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
nsv4450418	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 77,566,067-77,575,124 , GRCh38 chr13: 76,991,932-77,000,989	CLN5, FBXL3
nsv3883023	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 77,574,593-77,576,652 , GRCh38 chr13: 77,000,458-77,002,517	CLN5, FBXL3
nsv4681222	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 77,569,188-77,570,272 , GRCh38.p12 chr13: 76,995,053-76,996,137	CLN5, FBXL3
nsv3909761	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 77,574,552-77,575,350 , GRCh38.p12 chr13: 77,000,417-77,001,215	CLN5, FBXL3
nsv6309493	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr13: 77,566,176-77,566,487 , GRCh38 chr13: 76,992,041-76,992,352	CLN5, FBXL3
nsv4683977	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr13: 77,569,188-77,569,373 , GRCh38.p12 chr13: 76,995,053-76,995,238	CLN5, FBXL3
nsv7093499	delins	1	nstd102	human	Likely pathogenic	GRCh37 chr13: 77,569,985-77,570,062 , GRCh38 chr13: 76,995,850-76,995,927	CLN5, FBXL3
nsv4681578	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 77,566,067-77,575,124 , GRCh38.p12 chr13: 76,991,932-77,000,989	CLN5, FBXL3
nsv6309537	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 77,566,087-77,575,104 , GRCh38.p12 chr13: 76,991,952-77,000,969	CLN5, FBXL3
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	CLN5, RNU6-71P, 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	CLN5, LOC105370271, 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	CLN5, TEX30, 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	CLN5, GPC5, 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	CLN5, RNY4P30, 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	CLN5, SRSF1P1, 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	CLN5, RBM26, 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	CLN5, RPL21P108, 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	CLN5, ARL11, 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	CLN5, RNU7-88P, 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	CLN5, LINC00383, 359 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 73

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Number of Variants: 20

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Supplemental Content

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Search details

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