nsf[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
nsv3900923	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 44,662,268-44,782,177 , GRCh38.p12 chr17: 46,584,902-46,704,811 , GRCh38.p12 chr17\|NT_187663.1: 1,104,579-1,224,236	NSF, LRRC37A2
nsv3910262	copy number variation	1	nstd102	human	Benign	NCBI36 chr17: 41,841,216-42,114,094 , GRCh37 chr17: 44,485,800-44,758,915 , GRCh38 chr17: 46,444,520-46,681,549	NSF, ARL17A, 3 more genes
nsv3901331	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 44,628,880-44,782,177 , GRCh38.p12 chr17: 46,551,514-46,704,811 , GRCh38.p12 chr17\|NT_187663.1: 1,071,223-1,224,236	NSF, LRRC37A2, 2 more genes
nsv3908289	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 44,654,416-44,782,177 , GRCh38.p12 chr17: 46,577,050-46,704,811 , GRCh38.p12 chr17\|NT_187663.1: 1,096,717-1,224,236	NSF, LRRC37A2, 1 more genes
nsv3915338	copy number variation	1	nstd102	human	Benign	NCBI36 chr17: 41,841,187-42,049,599 , GRCh37 chr17: 44,485,771-44,694,283 , GRCh38 chr17: 46,444,520-46,661,960	NSF, FAM215B, 3 more genes
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	NSF, PRPSAP1, 1350 more genes
nsv3915599	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 41,012,476-42,049,627 , GRCh38 chr17: 45,579,327-46,661,960 , GRCh37 chr17: 43,656,693-44,694,311	NSF, LOC107985028, 29 more genes
nsv3909906	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 41,062,678-42,117,723 , GRCh37.p13 chr17: 43,706,895-44,762,543 , GRCh38.p12 chr17: 45,629,529-46,685,177	NSF, MAPT-IT1, 25 more genes
nsv3912268	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 45,629,520-46,661,960 , GRCh37 chr17: 43,706,886-44,694,283 , NCBI36 chr17: 41,062,669-42,049,599	NSF, LOC107985028, 25 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	NSF, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	NSF, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	NSF, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	NSF, SMURF2, 2366 more genes
nsv3914783	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577	NSF, LOC105371922, 1855 more genes
nsv3909511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846	NSF, FOXK2, 958 more genes
nsv3913552	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225	NSF, RNU6-131P, 1075 more genes
nsv3911563	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214	NSF, PLEKHH3, 958 more genes
nsv4676249	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 43,655,356-44,784,639 , GRCh38.p12 chr17: 45,577,990-46,707,273 , GRCh38.p12 chr17\|NT_187663.1: 280,129-1,226,699	NSF, KANSL1-AS1, 30 more genes
nsv3917213	copy number variation	1	nstd102	human	Benign	NCBI36 chr17: 41,710,482-42,142,827 , GRCh37.p13 chr17: 44,354,705-44,787,644 , GRCh38.p12 chr17: 46,277,339-46,710,278	NSF, LRRC37A, 7 more genes
nsv3912308	copy number variation	1	nstd102	human	Benign	NCBI36 chr17: 41,731,132-42,142,827 , GRCh37.p13 chr17: 44,375,355-44,787,644 , GRCh38.p12 chr17: 46,297,989-46,710,278	NSF, LRRC37A, 7 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 56

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Number of Variants: 20

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