baiap2l1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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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
nsv3904183	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 97,946,927-97,950,179 , GRCh38.p12 chr7: 98,317,615-98,320,867	BAIAP2L1, BRI3
nsv3903601	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 97,924,483-97,924,558 , GRCh38.p12 chr7: 98,295,171-98,295,246	BAIAP2L1, BRI3
nsv3878129	copy number variation	1	nstd102	human	not provided	GRCh37 chr7: 97,933,601-98,157,619 , GRCh38 chr7: 98,304,289-98,528,307	BAIAP2L1, RPS26P33, 3 more genes
esv3648373	copy number variation	1	estd216	human	not provided	GRCh37 chr7: 97,933,601-98,157,619 , GRCh38.p12 chr7: 98,304,289-98,528,307	BAIAP2L1, BRI3, 3 more genes
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	BAIAP2L1, 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	BAIAP2L1, LOC107986817, 2014 more genes
nsv3892887	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 92,445,452-99,686,985 , GRCh38.p12 chr7: 92,816,138-100,089,362	BAIAP2L1, LOC105375402, 153 more genes
nsv6636271	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 92,721,627-98,311,537 , GRCh38.p12 chr7: 93,092,314-98,682,225	BAIAP2L1, MARK2P10, 97 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	BAIAP2L1, 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	BAIAP2L1, 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	BAIAP2L1, 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	BAIAP2L1, TRGV3, 2682 more genes
nsv3922815	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 96,887,100-158,409,214 , GRCh38 chr7: 97,419,852-158,923,762 , GRCh37 chr7: 97,049,164-158,716,453	BAIAP2L1, SEPTIN7P6, 1175 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	BAIAP2L1, ARPC1A, 265 more genes
nsv3916333	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 97,917,786-100,903,085 , GRCh38 chr7: 98,288,474-101,259,804 , NCBI36 chr7: 97,755,722-100,689,805	BAIAP2L1, ZCWPW1, 141 more genes
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	BAIAP2L1, 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	BAIAP2L1, 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	BAIAP2L1, RRBP1P1, 2680 more genes
nsv6636406	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 97,786,282-98,313,434 , GRCh38.p12 chr7: 98,156,970-98,684,122	BAIAP2L1, RPS26P33, 9 more genes

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