lurap1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6310879	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 46,662,483-46,671,639 , GRCh38.p12 chr1: 46,196,811-46,205,967	LURAP1, TSPAN1, 1 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	LURAP1, 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	LURAP1, 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	LURAP1, RNU1-153P, 4887 more genes
nsv6313688	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139	LURAP1, LOC107984940, 407 more genes
nsv3888489	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr1: 45,303,358-52,157,856 , GRCh38.p12 chr1: 44,837,686-51,692,184	LURAP1, CDKN2C, 141 more genes
nsv3905377	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr1: 45,935,520-46,686,477 , GRCh38 chr1: 45,469,848-46,220,805 , NCBI36 chr1: 45,708,107-46,459,064	LURAP1, MMACHC, 23 more genes
nsv4453509	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 46,541,327-46,668,698 , GRCh38.p12 chr1: 46,075,655-46,203,026	LURAP1, POMGNT1, 5 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	LURAP1, LINC01776, 1853 more genes
nsv3889597	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 46,372,688-47,188,150 , GRCh38.p12 chr1: 45,907,016-46,722,478	LURAP1, NENFP1, 27 more genes
nsv3902893	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr1: 45,488,251-46,220,805 , NCBI36 chr1: 45,726,510-46,459,064 , GRCh37 chr1: 45,953,923-46,686,477	LURAP1, TESK2, 23 more genes
nsv6313850	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 46,083,531-46,738,006 , GRCh38.p12 chr1: 45,617,859-46,272,334	LURAP1, LOC105378694, 18 more genes
nsv3881303	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 46,078,097-46,725,770 , GRCh38.p12 chr1: 45,612,425-46,260,098	LURAP1, TMEM69, 18 more genes
nsv6290563	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 46,098,762-46,668,497 , GRCh38.p12 chr1: 45,633,090-46,202,825	LURAP1, POMGNT1, 15 more genes
nsv3882928	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 46,541,307-47,088,882 , GRCh38.p12 chr1: 46,075,635-46,623,210	LURAP1, PIK3R3, 19 more genes
nsv6636290	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 46,233,623-46,668,497 , GRCh38.p12 chr1: 45,767,951-46,202,825	LURAP1, TMA16P2, 9 more genes
nsv4674480	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 46,501,759-46,898,503 , GRCh38.p12 chr1: 46,036,087-46,432,831	LURAP1, LRRC41, 12 more genes

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