ifrd1[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
nsv3892800	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 112,094,085-112,140,430 , GRCh38.p12 chr7: 112,454,030-112,500,375	IFRD1, LSMEM1
nsv3898812	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 112,094,085-112,128,978 , GRCh38.p12 chr7: 112,454,030-112,488,923	IFRD1, LSMEM1
nsv4456575	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 112,092,779-112,333,402 , GRCh38.p12 chr7: 112,452,724-112,693,347	IFRD1, LSMEM1, 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	IFRD1, 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	IFRD1, 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	IFRD1, 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	IFRD1, 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	IFRD1, CBLL1-AS1, 168 more genes
nsv3900620	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 111,613,396-127,897,316 , GRCh38.p12 chr7: 111,973,341-128,257,263	IFRD1, LSM8, 170 more genes
nsv3923570	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 107,583,881-122,963,817 , GRCh37.p13 chr7: 107,796,645-123,176,581 , GRCh38.p12 chr7: 108,156,200-123,536,527	IFRD1, ANKRD7, 142 more genes
nsv4455557	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,410,314-117,825,549 , GRCh38.p12 chr7: 107,769,869-118,185,495	IFRD1, RAC1P6, 103 more genes
nsv3882930	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 111,781,517-120,142,536 , GRCh37.p13 chr7: 111,994,281-120,355,300 , GRCh38.p12 chr7: 112,354,226-120,715,246	IFRD1, LOC105375472, 78 more genes
nsv3877875	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 108,290,244-114,759,023 , GRCh37.p13 chr7: 108,503,008-114,971,787 , GRCh38.p12 chr7: 108,862,564-115,331,733	IFRD1, GPR85, 43 more genes
nsv3891918	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 111,642,645-115,770,275 , GRCh38.p12 chr7: 112,002,590-116,130,221	IFRD1, FOXP2, 33 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	IFRD1, 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	IFRD1, 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	IFRD1, 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	IFRD1, 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	IFRD1, 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	IFRD1, CYP3A5, 1144 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 41

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Number of Variants: 20

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Supplemental Content

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