tmem243[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3894751	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 86,826,422-86,885,119 , GRCh38.p12 chr7: 87,197,106-87,255,803	TMEM243, LOC105375384
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	TMEM243, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	TMEM243, LOC107986817, 2014 more genes
nsv3914094	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 84,002,634-95,228,883 , GRCh37 chr7: 83,631,950-94,858,195 , NCBI36 chr7: 83,469,886-94,696,131	TMEM243, LINC03017, 121 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	TMEM243, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	TMEM243, RPL23AP51, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	TMEM243, MNX1-AS2, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	TMEM243, TRGV3, 2682 more genes
nsv6313801	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 77,821,356-93,340,137 , GRCh38.p12 chr7: 78,192,039-93,710,825	TMEM243, SOCS5P1, 140 more genes
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	TMEM243, AOC1, 2682 more genes
nsv4352523	inversion	1	nstd102	human	Pathogenic	GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550	TMEM243, ACHE, 1532 more genes
nsv6634332	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635	TMEM243, RRBP1P1, 2680 more genes
nsv3873500	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 73,591,993-93,683,437 , GRCh38.p12 chr7: 74,177,663-94,054,125	TMEM243, LOC645324, 242 more genes
nsv4728924	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 86,833,114-87,553,208 , GRCh38.p12 chr7: 87,203,798-87,923,893	TMEM243, ABCB1, 7 more genes
nsv3918429	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr7: 86,669,909-87,492,659 , NCBI36 chr7: 86,137,161-86,959,911 , GRCh37 chr7: 86,299,225-87,121,975	TMEM243, ELAPOR2, 8 more genes

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