ints2[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
nsv4729942	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 59,867,228-59,995,992 , GRCh38.p12 chr17: 61,789,867-61,918,631	INTS2, BRIP1
nsv7094910	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 59,861,718-59,940,920 , GRCh38.p12 chr17: 61,784,357-61,863,559	INTS2, BRIP1
nsv3870474	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr17: 59,756,547-59,940,920 , GRCh38.p12 chr17: 61,679,186-61,863,559	INTS2, BRIP1
nsv4769397	delins	1	nstd102	human	Pathogenic	GRCh37 chr17: 59,937,844-59,940,820 , GRCh38 chr17: 61,860,483-61,863,459	INTS2, BRIP1
nsv6291829	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr17: 61,778,623-62,006,540 , GRCh37.p13 chr17: 59,855,984-60,083,901	INTS2, BRIP1, 2 more genes
nsv3912471	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr17: 57,245,616-57,458,469 , GRCh37 chr17: 59,890,834-60,103,687 , GRCh38 chr17: 61,813,473-62,026,326	INTS2, MED13, 2 more genes
nsv3896096	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 59,815,184-60,231,398 , GRCh38.p12 chr17: 61,737,823-62,154,037	INTS2, BRIP1, 3 more genes
nsv3921043	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr17: 57,291,907-57,375,837 , GRCh38 chr17: 61,859,764-61,943,694 , GRCh37 chr17: 59,937,125-60,021,055	INTS2, BRIP1, 1 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	INTS2, PRPSAP1, 1350 more genes
nsv3895056	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 56,623,275-60,285,107 , GRCh38.p12 chr17: 58,545,914-62,207,746	INTS2, MIR454, 87 more genes
nsv3918670	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 58,172,700-60,315,303 , GRCh38 chr17: 60,095,339-62,237,942 , NCBI36 chr17: 55,527,482-57,670,085	INTS2, MED13, 37 more genes
nsv3916375	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 55,475,591-57,580,872 , GRCh38 chr17: 60,043,448-62,148,729 , GRCh37 chr17: 58,120,809-60,226,090	INTS2, HEATR6-DT, 41 more genes
nsv3911620	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 58,332,553-60,315,303 , GRCh38 chr17: 60,255,192-62,237,942 , NCBI36 chr17: 55,687,335-57,670,085	INTS2, CHCT1, 31 more genes
nsv3901406	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 58,934,659-60,395,826 , NCBI36 chr17: 56,289,441-57,750,608 , GRCh38.p12 chr17: 60,857,298-62,318,465	INTS2, TBX4, 18 more genes
nsv3318990	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr17: 58,113,002-60,275,809 , GRCh38.p12 chr17: 60,035,641-62,198,448	INTS2, CA4, 41 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	INTS2, 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	INTS2, 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	INTS2, 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	INTS2, 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	INTS2, LOC105371922, 1855 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 33

Page of 2

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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