tnpo1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3917943	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 71,906,759-72,199,095 , GRCh37.p13 chr5: 71,871,003-72,163,339 , GRCh38.p12 chr5: 72,575,176-72,867,512	TNPO1, H2BL1P, 1 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	TNPO1, MEGF10, 2080 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	TNPO1, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	TNPO1, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	TNPO1, SPEF2, 2490 more genes
nsv3911585	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550	TNPO1, LINC02241, 878 more genes
nsv4578696	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr5: 58,780,641-73,523,380 , GRCh37.p13 chr5: 58,076,468-72,819,205	TNPO1, TRIM23, 215 more genes
nsv3875351	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 72,129,604-72,354,897 , GRCh38.p12 chr5: 72,833,777-73,059,070	TNPO1, MIR4804, 4 more genes
nsv4436202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379	TNPO1, RNU1-150P, 1757 more genes
nsv3912593	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259	TNPO1, LOC105378993, 2492 more genes
nsv4455596	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr5: 71,721,970-72,431,813 , GRCh38.p12 chr5: 72,426,143-73,135,986	TNPO1, TMEM171, 10 more genes

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