upp2[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
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	UPP2, DAZAP2P1, 2991 more genes
nsv3898306	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 148,917,286-163,204,623 , GRCh37 chr2: 149,674,855-164,061,133 , NCBI36 chr2: 149,391,325-163,769,379	UPP2, RPS3AP13, 170 more genes
nsv3877758	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 157,970,774-169,270,675 , GRCh38.p12 chr2: 157,114,262-168,414,165	UPP2, GCA, 121 more genes
nsv3921316	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 155,624,215-165,414,901 , GRCh37.p13 chr2: 155,915,969-165,706,655 , GRCh38.p12 chr2: 155,059,457-164,850,145	UPP2, LOC105373712, 121 more genes
nsv3894168	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 152,788,858-160,276,245 , GRCh38 chr2: 151,932,344-159,419,734 , NCBI36 chr2: 152,497,104-159,984,491	UPP2, RNU6-1001P, 88 more genes
nsv3910092	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 152,138,015-159,100,037 , GRCh37.p13 chr2: 152,429,769-159,391,791 , GRCh38.p12 chr2: 151,573,255-158,535,279	UPP2, ACVR1C, 73 more genes
nsv6313568	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 158,950,827-164,456,735 , GRCh38.p12 chr2: 158,094,315-163,600,225	UPP2, PSMD14-DT, 70 more genes
nsv3922653	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 154,499,404-159,392,834 , GRCh37.p13 chr2: 154,791,158-159,684,588 , GRCh38.p12 chr2: 153,934,645-158,828,076	UPP2, CCDC148, 59 more genes
nsv3892461	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 154,466,227-159,041,637 , GRCh38 chr2: 153,609,714-158,185,125 , NCBI36 chr2: 154,174,473-158,749,883	UPP2, RNU6-1001P, 53 more genes
nsv6291000	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 154,852,961-159,126,250 , GRCh38.p12 chr2: 153,996,448-158,269,738	UPP2, LINC01876, 52 more genes
nsv4674584	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 158,925,958-162,489,191 , GRCh38.p12 chr2: 158,069,446-161,632,681	UPP2, RPS3AP13, 50 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	UPP2, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	UPP2, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	UPP2, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	UPP2, MTND2P22, 3724 more genes
nsv3875392	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 152,409,978-179,325,736 , GRCh38.p12 chr2: 151,553,464-178,461,009	UPP2, MIR10B, 359 more genes
nsv3874278	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 156,489,430-182,921,298 , GRCh38.p12 chr2: 155,632,918-182,056,571	UPP2, LOC107985957, 358 more genes
nsv3893853	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 154,294,042-175,989,372 , GRCh37 chr2: 155,150,555-176,854,100 , NCBI36 chr2: 154,858,801-176,562,346	UPP2, SCN7A, 275 more genes
nsv3904897	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 143,900,149-158,321,624 , GRCh37 chr2: 144,657,717-159,178,136 , NCBI36 chr2: 144,374,187-158,886,382	UPP2, RPLP0P7, 149 more genes
nsv3902725	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 154,931,546-167,613,658 , GRCh38 chr2: 154,366,788-167,048,902 , GRCh37 chr2: 155,223,300-167,905,412	UPP2, SCN2A, 148 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 28

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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