yars1[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
nsv7095526	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 33,256,743-33,272,232 , GRCh38.p12 chr1: 32,791,142-32,806,631	YARS1
nsv7095990	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 33,246,629-33,248,160 , GRCh38.p12 chr1: 32,781,028-32,782,559	YARS1
nsv6314808	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 33,251,953-33,252,686 , GRCh38.p12 chr1: 32,786,352-32,787,085	YARS1
nsv6314842	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 33,276,172-33,276,678 , GRCh38.p12 chr1: 32,810,571-32,811,077	YARS1
nsv4682965	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 33,276,182-33,276,668 , GRCh38.p12 chr1: 32,810,581-32,811,067	YARS1
nsv3888014	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr1: 32,810,591-32,811,057 , GRCh37 chr1: 33,276,192-33,276,658	YARS1
nsv7095525	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 33,247,985-33,248,160 , GRCh38.p12 chr1: 32,782,384-32,782,559	YARS1
nsv4682512	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 33,241,572-33,263,454 , GRCh38.p12 chr1: 32,775,971-32,797,853	YARS1
nsv6314843	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 33,276,172-33,282,845 , GRCh38.p12 chr1: 32,810,571-32,817,244	YARS1, S100PBP
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	YARS1, SNHG3, 115 more genes
nsv4346788	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 32,859,415-36,454,915 , GRCh38.p12 chr1: 32,393,814-35,989,314	YARS1, LOC100419802, 75 more genes
nsv3895257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 31,239,605-33,825,029 , NCBI36 chr1: 31,012,192-33,597,616 , GRCh38 chr1: 30,766,758-33,359,428	YARS1, LOC105378623, 85 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	YARS1, 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	YARS1, 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	YARS1, 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	YARS1, TMEM222, 453 more genes
nsv3874782	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 31,562,164-37,421,958 , GRCh38.p12 chr1: 31,089,317-36,956,357	YARS1, LOC101929444, 143 more genes
nsv4674454	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr1: 30,819,875-34,380,419 , GRCh38.p12 chr1: 30,347,028-33,914,818	YARS1, AK2, 97 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	YARS1, LINC01776, 1853 more genes
nsv3878135	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 33,241,563-46,663,513 , GRCh38.p12 chr1: 32,775,962-46,197,841	YARS1, LINC02786, 365 more genes

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Items: 20

Number of Variants: 20

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