ccdc71l[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

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	CCDC71L, 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	CCDC71L, LOC107986817, 2014 more genes
nsv3924380	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 101,912,320-120,918,695 , GRCh38 chr7: 102,196,924-121,278,641 , NCBI36 chr7: 101,626,924-120,705,931	CCDC71L, LOC102724434, 222 more genes
nsv6313576	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106	CCDC71L, LHFPL3-AS2, 233 more genes
nsv6313503	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253	CCDC71L, GJC3, 237 more genes
nsv3912378	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 101,807,149-112,414,850 , GRCh37 chr7: 101,450,429-112,054,905 , NCBI36 chr7: 101,237,149-111,842,141	CCDC71L, DNAJC2, 139 more genes
nsv3913401	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 105,902,385-110,868,092 , GRCh38 chr7: 106,261,939-111,228,036 , NCBI36 chr7: 105,689,621-110,655,328	CCDC71L, DUS4L-BCAP29, 52 more genes
nsv7097853	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 104,456,677-108,155,935 , GRCh38.p12 chr7: 104,816,230-108,515,491	CCDC71L, RNU6-1322P, 57 more genes
nsv4578664	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 104,506,008-107,408,857 , GRCh38.p12 chr7: 104,865,561-107,768,412	CCDC71L, LHFPL3-AS2, 43 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	CCDC71L, 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	CCDC71L, 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	CCDC71L, 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	CCDC71L, 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	CCDC71L, SEPTIN7P6, 1175 more genes
nsv3894097	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 98,693,388-159,119,707 , GRCh38.p12 chr7: 99,095,765-159,327,017	CCDC71L, CYP3A5, 1144 more genes
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	CCDC71L, 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	CCDC71L, 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	CCDC71L, RRBP1P1, 2680 more genes
nsv3920319	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr7: 105,575,647-107,949,294 , NCBI36 chr7: 105,003,330-107,376,975 , GRCh37 chr7: 105,216,094-107,589,739	CCDC71L, LOC105375444, 35 more genes
nsv7097099	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 102,937,907-107,643,330 , GRCh38.p12 chr7: 103,297,460-108,002,885	CCDC71L, SRPK2, 60 more genes

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Items: 20

Number of Variants: 20

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