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

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Items: 13

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3891775	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 29,460,082-30,077,300 , GRCh37 chr1: 29,587,495-30,304,713 , GRCh38 chr1: 29,260,983-29,831,866	PTPRU, LOC107984933, 2 more genes
nsv4453440	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 29,490,892-29,581,035 , GRCh38.p12 chr1: 29,164,380-29,254,523	PTPRU, SRSF4, 1 more genes
nsv3891425	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 28,623,965-33,361,042 , GRCh37 chr1: 28,751,378-33,588,455 , GRCh38 chr1: 28,424,867-33,122,854	PTPRU, SNHG3, 115 more genes
nsv3892157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 29,600,988-31,598,923 , GRCh38 chr1: 29,274,476-31,126,076 , NCBI36 chr1: 29,473,575-31,371,510	PTPRU, SNORD103B, 23 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	PTPRU, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	PTPRU, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	PTPRU, RNU1-153P, 4887 more genes
nsv3901163	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 24,707,696-41,886,350 , GRCh38 chr1: 24,381,206-41,401,517 , NCBI36 chr1: 24,580,283-41,658,937	PTPRU, TMEM222, 453 more genes
nsv3907483	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 27,289,536-32,744,646 , GRCh38 chr1: 26,963,045-32,279,045 , NCBI36 chr1: 27,162,123-32,517,233	PTPRU, ATP5IF1, 138 more genes
nsv4674576	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 29,293,936-30,478,996 , GRCh38.p12 chr1: 28,967,424-30,006,149	PTPRU, MECR, 7 more genes
nsv4436181	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532	PTPRU, LINC01776, 1853 more genes
nsv6313753	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 27,543,877-32,819,121 , GRCh38.p12 chr1: 27,217,386-32,353,520	PTPRU, DCDC2B, 130 more genes
nsv3902515	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr1: 29,015,141-30,983,083 , GRCh37 chr1: 29,341,653-31,455,930 , NCBI36 chr1: 29,214,240-31,228,517	PTPRU, PUM1, 24 more genes

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ptpru[All Fields] AND 1[has_clinical] (14)
dbVar
Prevention of contrast media-induced nephropathy by isotonic sodium bicarbonate:...
Prevention of contrast media-induced nephropathy by isotonic sodium bicarbonate: a meta-analysis - Database of Abstracts of Reviews of Effects (DARE): Quality-assessed Reviews

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