ND4L[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5674221	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrMT: 6,468-15,586 , GRCh37 chrMT: 6,468-15,586	ND4L, ND5, 20 more genes
nsv5674222	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrMT: 7,126-13,988 , GRCh37 chrMT: 7,126-13,988	ND4L, TRNH, 20 more genes
nsv4685968	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrMT: 8,839-14,895 , GRCh38 chrMT: 8,839-14,895	ND4L, TRNG, 16 more genes
nsv4685928	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrMT: 6,003-11,220 , GRCh37 chrMT: 6,003-11,220	ND4L, COX2, 21 more genes
nsv4685910	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrMT: 8,350-13,450 , GRCh38 chrMT: 8,350-13,450	ND4L, TRNK, 15 more genes
nsv5674153	copy number variation	2	nstd102	human	not provided, Pathogenic	GRCh37 chrMT: 8,470-13,446 , GRCh38 chrMT: 8,470-13,446	ND4L, ND4, 15 more genes
nsv5674171	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrMT: 10,105-15,066 , GRCh38 chrMT: 10,105-15,066	ND4L, COX3, 13 more genes
nsv4685954	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrMT: 8,480-13,440 , GRCh37 chrMT: 8,480-13,440	ND4L, COX2, 15 more genes
nsv4685933	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrMT: 8,815-13,722 , GRCh38 chrMT: 8,815-13,722	ND4L, CYTB, 14 more genes
nsv4685959	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrMT: 8,290-13,040 , GRCh37 chrMT: 8,290-13,040	ND4L, CYTB, 15 more genes
nsv7098831	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrMT: 10,947-15,537 , GRCh38 chrMT: 10,947-15,537	ND4L, TRNS2, 10 more genes
nsv5674154	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrMT: 8,585-12,965 , GRCh38 chrMT: 8,585-12,965	ND4L, ATP6, 15 more genes
nsv4685897	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrMT: 11,263-15,374 , GRCh37 chrMT: 11,263-15,374	ND4L, TRNE, 9 more genes
nsv4685892	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrMT: 7,730-11,255 , GRCh38 chrMT: 7,730-11,255	ND4L, TRNG, 15 more genes
nsv4685966	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrMT: 5,794-14,876 , GRCh38 chrMT: 5,794-14,876	ND4L, ATP6, 26 more genes
nsv4685879	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrMT: 5,782-13,922 , GRCh38 chrMT: 5,782-13,922	ND4L, ATP6, 25 more genes

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