trim65[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
nsv3890185	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 73,875,481-73,885,805 , GRCh38.p12 chr17: 75,879,400-75,889,724	TRIM65
nsv3893184	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 73,875,481-73,878,937 , GRCh38.p12 chr17: 75,879,400-75,882,856	TRIM65
nsv3893908	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 73,875,838-73,878,937 , GRCh38.p12 chr17: 75,879,757-75,882,856	TRIM65
nsv3899927	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 73,872,539-73,888,439 , GRCh38.p12 chr17: 75,876,458-75,892,358	TRIM65, TRIM47
nsv3904069	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 73,873,656-73,886,888 , GRCh38.p12 chr17: 75,877,575-75,890,807	TRIM65, TRIM47
nsv3897135	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 73,872,539-73,922,221 , GRCh38.p12 chr17: 75,876,458-75,926,140	TRIM65, FBF1, 2 more genes
nsv3894017	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 73,872,948-73,922,221 , GRCh38.p12 chr17: 75,876,867-75,926,140	TRIM65, TRIM47, 2 more genes
nsv3905530	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 73,871,467-73,897,977 , GRCh38.p12 chr17: 75,875,386-75,901,896	TRIM65, TRIM47, 1 more genes
nsv3906829	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 73,871,467-73,895,007 , GRCh38.p12 chr17: 75,875,386-75,898,926	TRIM65, MRPL38, 1 more genes
nsv3895893	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 73,886,097-73,914,116 , GRCh38.p12 chr17: 75,890,016-75,918,035	TRIM65, FBF1, 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	TRIM65, PRPSAP1, 1350 more genes
nsv3919795	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 71,144,026-71,478,420 , GRCh37 chr17: 73,632,431-73,966,825 , GRCh38 chr17: 75,636,351-75,970,744	TRIM65, ITGB4, 15 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	TRIM65, 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	TRIM65, 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	TRIM65, 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	TRIM65, 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	TRIM65, 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	TRIM65, FOXK2, 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	TRIM65, 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	TRIM65, RPL38, 428 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 31

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Number of Variants: 20

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Supplemental Content

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