csk[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
nsv6291818	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 75,047,425-75,073,422 , GRCh38.p12 chr15: 74,755,084-74,781,081	CSK, CYP1A2
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	CSK, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	CSK, RNU6-18P, 1442 more genes
nsv3913942	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 70,025,300-78,705,993 , NCBI36 chr15: 68,104,693-76,785,390 , GRCh37 chr15: 70,317,639-78,998,335	CSK, SNX33, 209 more genes
nsv6637477	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 74,353,736-77,884,397 , GRCh38.p12 chr15: 74,061,395-77,592,055	CSK, PTPN9, 96 more genes
nsv7137210	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,943,184-76,085,232 , GRCh38.p12 chr15: 72,650,843-75,792,891	CSK, LOC105370892, 99 more genes
nsv3895410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,943,184-76,072,324 , GRCh38.p12 chr15: 72,650,843-75,779,983	CSK, UBL7-DT, 97 more genes
nsv3920020	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 72,685,231-75,727,625 , NCBI36 chr15: 70,764,625-73,807,021 , GRCh37 chr15: 72,977,572-76,019,966	CSK, STRA6, 91 more genes
nsv3914896	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,963,970-75,954,617 , GRCh38 chr15: 72,671,629-75,662,276 , NCBI36 chr15: 70,751,023-73,741,672	CSK, CYP1A1, 88 more genes
nsv6309590	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,978,569-75,722,716 , GRCh38.p12 chr15: 72,686,228-75,430,375	CSK, NPM1P42, 82 more genes
nsv3905553	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr15: 72,943,184-75,567,198 , GRCh38.p12 chr15: 72,650,843-75,274,857	CSK, SEMA7A, 74 more genes
nsv4455687	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,926,922-75,544,524 , GRCh38.p12 chr15: 72,634,581-75,252,183	CSK, SCAMP2, 74 more genes
nsv3903760	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,958,539-75,569,605 , GRCh38.p12 chr15: 72,666,198-75,277,264	CSK, LOC105370893, 73 more genes
nsv3888972	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,958,539-75,569,605 , GRCh38.p12 chr15: 72,666,198-75,277,264	CSK, NEO1, 73 more genes
nsv4455940	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,943,184-75,544,524 , GRCh38.p12 chr15: 72,650,843-75,252,183	CSK, TBC1D21, 72 more genes
nsv3914282	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 70,751,023-73,322,383 , GRCh37 chr15: 72,963,970-75,535,330 , GRCh38 chr15: 72,671,629-75,242,989	CSK, CLK3, 69 more genes
nsv6315505	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 74,398,068-76,054,094 , GRCh38.p12 chr15: 74,105,727-75,761,753	CSK, RPL36AP45, 62 more genes
nsv4729106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 74,398,162-76,054,094 , GRCh38.p12 chr15: 74,105,821-75,761,753	CSK, FAM219B, 62 more genes
nsv3911951	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 72,186,358-73,827,604 , GRCh37.p13 chr15: 74,399,305-76,040,549 , GRCh38.p12 chr15: 74,106,964-75,748,208	CSK, NEIL1, 60 more genes
nsv3895297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 75,078,195-75,862,756 , GRCh38.p12 chr15: 74,785,854-75,570,415	CSK, FAM219B, 33 more genes

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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 51

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Number of Variants: 20

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