bptf[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
nsv3898280	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 65,962,298-65,980,635 , GRCh38.p12 chr17: 67,966,182-67,984,519	BPTF, RN7SL622P
nsv3883721	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 65,898,399-65,986,986 , GRCh38.p12 chr17: 67,902,283-67,990,870	BPTF, C17orf58, 1 more genes
nsv3898709	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 65,962,298-65,990,392 , GRCh38.p12 chr17: 67,966,182-67,994,276	BPTF, RN7SL622P, 1 more genes
nsv3897056	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 65,962,298-65,990,341 , GRCh38.p12 chr17: 67,966,182-67,994,225	BPTF, RN7SL622P, 1 more genes
nsv4729867	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 65,709,215-65,952,716 , GRCh38.p12 chr17: 67,713,099-67,956,600	BPTF, NOL11, 4 more genes
nsv3889416	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 65,700,189-65,896,342 , GRCh38.p12 chr17: 67,704,073-67,900,226	BPTF, NOL11, 4 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	BPTF, PRPSAP1, 1350 more genes
nsv3921398	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 65,829,982-68,081,995 , GRCh38 chr17: 67,833,866-70,085,854 , NCBI36 chr17: 63,260,444-65,593,590	BPTF, LRRC37A16P, 41 more genes
nsv3920127	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 67,584,224-68,639,875 , NCBI36 chr17: 63,010,802-64,147,611 , GRCh37 chr17: 65,580,340-66,636,016	BPTF, LOC101928045, 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	BPTF, 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	BPTF, 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	BPTF, 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	BPTF, 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	BPTF, 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	BPTF, 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	BPTF, 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	BPTF, PLEKHH3, 958 more genes
nsv4457646	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062	BPTF, LOC107985089, 448 more genes
nsv3909523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062	BPTF, RPL38, 428 more genes
nsv4457799	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 57,869,604-67,078,443 , GRCh38.p12 chr17: 59,792,243-69,082,302	BPTF, PECAM1, 215 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 23

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Number of Variants: 20

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Supplemental Content

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Search details

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