trim28[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 12

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	TRIM28, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	TRIM28, BABAM1, 2426 more genes
nsv3919076	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,432,832-59,083,573 , NCBI36 chr19: 53,124,644-63,775,385 , GRCh38 chr19: 47,929,575-58,572,206	TRIM28, KCNA7, 697 more genes
nsv3924732	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 49,907,832-58,557,889 , GRCh37 chr19: 50,411,089-59,069,256 , NCBI36 chr19: 55,102,901-63,761,068	TRIM28, RPL39P37, 556 more genes
nsv3890862	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 50,489,390-59,095,359 , GRCh38.p12 chr19: 49,986,133-58,583,992	TRIM28, SIGLECL1, 552 more genes
nsv3923909	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 55,347,589-63,784,382 , GRCh37 chr19: 50,655,777-59,092,570 , GRCh38 chr19: 50,152,520-58,581,203	TRIM28, OSCAR, 535 more genes
nsv3891963	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 50,740,074-59,097,160 , GRCh38.p12 chr19: 50,236,817-58,585,793	TRIM28, RPS9, 535 more genes
nsv3923613	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 52,612,432-58,581,203 , GRCh37 chr19: 53,115,685-59,092,570 , NCBI36 chr19: 57,807,497-63,784,382	TRIM28, ZNF71-SMIM17, 393 more genes
nsv3919766	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 58,150,121-63,784,382 , GRCh37 chr19: 53,458,309-59,092,570 , GRCh38 chr19: 52,955,056-58,581,203	TRIM28, MIR520F, 382 more genes
nsv3916295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 61,566,389-63,784,382 , GRCh37 chr19: 56,874,577-59,092,570 , GRCh38 chr19: 56,363,208-58,581,203	TRIM28, ZIM2, 131 more genes
nsv3910645	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr19: 58,918,650-59,092,496 , NCBI36 chr19: 63,610,462-63,784,308 , GRCh38 chr19: 58,407,283-58,581,129	TRIM28, ZNF132, 18 more genes
nsv3922528	copy number variation	1	nstd102	human	Benign	NCBI36 chr19: 63,752,020-63,784,382 , GRCh37 chr19: 59,060,208-59,092,570 , GRCh38 chr19: 58,548,841-58,581,203	TRIM28, UBE2M, 5 more genes

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