cldn12[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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	CLDN12, 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	CLDN12, 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	CLDN12, 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	CLDN12, 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	CLDN12, 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	CLDN12, 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	CLDN12, 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	CLDN12, SOCS5P1, 140 more genes
nsv5381780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704	CLDN12, ARPC1A, 265 more genes
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	CLDN12, 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	CLDN12, ACHE, 1532 more genes
nsv3917092	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr7: 86,846,728-91,199,124 , GRCh37 chr7: 87,008,792-91,361,188 , GRCh38 chr7: 87,379,476-91,731,873	CLDN12, CDK14, 44 more genes
nsv3920135	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr7: 88,030,801-89,950,219 , GRCh37.p13 chr7: 88,192,865-90,112,283 , GRCh38.p12 chr7: 88,563,550-90,482,969	CLDN12, LOC107986816, 20 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	CLDN12, 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	CLDN12, LOC645324, 242 more genes
nsv4675401	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 88,533,008-90,192,559 , GRCh38.p12 chr7: 88,903,694-90,563,245	CLDN12, LOC101927446, 15 more genes
nsv1398043	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 87,840,219-91,707,100 , GRCh38.p12 chr7: 88,210,904-92,077,786	CLDN12, TEX47, 38 more genes
nsv3922902	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr7: 89,348,003-90,356,089 , GRCh37 chr7: 89,510,067-90,518,153 , GRCh38 chr7: 89,880,753-90,888,838	CLDN12, PTTG1IP2, 13 more genes
nsv3920942	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 89,515,649-90,376,577 , GRCh38 chr7: 89,886,335-90,747,262 , NCBI36 chr7: 89,353,585-90,214,513	CLDN12, TVP23CP1, 13 more genes

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