atp5if1[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
nsv3872050	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 28,517,625-28,633,254 , GRCh38.p12 chr1: 28,191,114-28,306,743 , GRCh38.p12 chr1\|NW_018654706.1: 1-100,387	ATP5IF1, DNAJC8, 2 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	ATP5IF1, 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	ATP5IF1, 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	ATP5IF1, 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	ATP5IF1, 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	ATP5IF1, LOC102723760, 138 more genes
nsv6290388	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 28,493,687-29,242,679 , GRCh38.p12 chr1: 28,167,176-28,916,167	ATP5IF1, SNORA16A, 24 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	ATP5IF1, 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	ATP5IF1, DCDC2B, 130 more genes
nsv3894712	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 28,245,710-28,933,738 , GRCh38 chr1: 27,919,199-28,607,226 , NCBI36 chr1: 28,118,297-28,806,325	ATP5IF1, SNHG12, 26 more genes
nsv3870497	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 28,292,253-28,969,539 , GRCh38.p12 chr1: 27,965,742-28,643,027	ATP5IF1, SNORA44, 26 more genes

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