dus4l[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
nsv6312421	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,002,458-107,204,434 , GRCh38.p12 chr7: 107,362,013-107,563,989 , GRCh38.p12 chr7\|NW_017852930.1: 207,539-409,644	DUS4L, COG5, 3 more genes
nsv7097101	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,188,536-107,204,434 , GRCh38.p12 chr7: 107,548,091-107,563,989 , GRCh38.p12 chr7\|NW_017852930.1: 393,746-409,644	DUS4L, COG5, 1 more genes
nsv6312518	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,204,228-107,204,434 , GRCh38.p12 chr7: 107,563,783-107,563,989 , GRCh38.p12 chr7\|NW_017852930.1: 409,438-409,644	DUS4L, COG5, 1 more genes
nsv3887149	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 107,262,480-107,286,241 , GRCh38 chr7: 107,622,035-107,645,796	BCAP29, WBP1LP2, 2 more genes
nsv3896814	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 107,156,793-107,222,725 , GRCh38.p12 chr7\|NW_017852930.1: 362,003-427,935 , GRCh38.p12 chr7: 107,516,348-107,582,280	DUS4L, DUS4L-BCAP29, 2 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	DUS4L, 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	DUS4L, 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	DUS4L, 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	DUS4L, LHFPL3-AS2, 233 more genes
nsv4675322	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 106,617,406-123,217,914 , GRCh38.p12 chr7: 106,976,961-123,577,860	DUS4L, CBLL1-AS1, 168 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	DUS4L, 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	DUS4L, 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	DUS4L, 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	DUS4L, 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	DUS4L, 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	DUS4L, 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	DUS4L, 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	DUS4L, 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	DUS4L, 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	DUS4L, SEPTIN7P6, 1175 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 27

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Number of Variants: 20

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