appbp2[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
nsv3893030	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 58,579,726-58,580,231 , GRCh38.p12 chr17: 60,502,365-60,502,870	APPBP2
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	APPBP2, 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	APPBP2, 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	APPBP2, 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	APPBP2, 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	APPBP2, INTS2, 31 more genes
nsv6291649	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 57,605,300-59,389,547 , GRCh38.p12 chr17: 59,527,939-61,312,186	APPBP2, RNU4-13P, 48 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	APPBP2, 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	APPBP2, 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	APPBP2, 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	APPBP2, 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	APPBP2, 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	APPBP2, 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	APPBP2, 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	APPBP2, 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	APPBP2, PLEKHH3, 958 more genes
nsv3890268	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 49,076,980-58,740,945 , GRCh38.p12 chr17: 50,999,619-60,663,584	APPBP2, NDUFB8P2, 161 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	APPBP2, PECAM1, 215 more genes
nsv4349383	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 57,357,088-66,306,668 , GRCh38.p12 chr17: 59,279,727-68,310,527	APPBP2, FAM136DP, 214 more genes
nsv3895703	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 56,321,134-62,080,001 , GRCh38.p12 chr17: 58,243,773-64,002,641	APPBP2, GH2, 161 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 29

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Number of Variants: 20

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Supplemental Content

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