mtfr1l[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3873536	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 26,146,392-26,146,514 , GRCh38.p12 chr1: 25,819,901-25,820,023	MTFR1L, LOC646471
nsv5673254	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 25,870,180-26,795,632 , GRCh38.p12 chr1: 25,543,689-26,469,141	MTFR1L, LDLRAP1, 36 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	MTFR1L, 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	MTFR1L, 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	MTFR1L, 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	MTFR1L, TMEM222, 453 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	MTFR1L, LINC01776, 1853 more genes
nsv7095609	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 25,870,190-27,278,871 , GRCh38.p12 chr1: 25,543,699-26,952,380	MTFR1L, RPL34P4, 53 more genes
nsv3904673	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 25,568,289-26,139,868 , GRCh37 chr1: 25,695,702-26,267,281 , GRCh38 chr1: 25,369,211-25,940,790	MTFR1L, MIR3917, 13 more genes
nsv4684184	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 25,872,197-26,274,156 , GRCh38.p12 chr1: 25,545,706-25,947,665	MTFR1L, MAN1C1, 10 more genes

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