rbm20[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
nsv6308900	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 112,540,539-112,583,392 , GRCh38.p12 chr10: 110,780,781-110,823,634	RBM20
nsv4455012	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr10: 110,780,791-110,823,624 , GRCh37 chr10: 112,540,549-112,583,382	RBM20
nsv4681125	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 112,579,820-112,595,746 , GRCh38.p12 chr10: 110,820,062-110,835,988	RBM20
nsv4451102	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr10: 110,780,781-110,835,998 , GRCh37 chr10: 112,540,539-112,595,756	RBM20
nsv3889915	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 112,579,810-112,595,756 , GRCh38 chr10: 110,820,052-110,835,998	RBM20
nsv6315483	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 112,516,278-112,591,134 , GRCh38.p12 chr10: 110,756,520-110,831,376	RBM20, RNA5SP327, 1 more genes
nsv3906619	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 112,559,414-112,668,381 , GRCh38.p12 chr10: 110,799,656-110,908,623	RBM20, PDCD4-AS1, 3 more genes
nsv3871649	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr10: 110,644,435-110,823,634 , GRCh37 chr10: 112,404,193-112,583,392	RBM20, RNA5SP327, 1 more genes
nsv4456676	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 112,448,209-112,601,330 , GRCh38.p12 chr10: 110,688,451-110,841,572	RBM20, RN7SKP288, 1 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	RBM20, RNU7-12P, 1876 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	RBM20, EIF2S2P3, 895 more genes
nsv3919820	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 107,191,100-118,761,489 , GRCh37 chr10: 108,950,858-120,521,001 , NCBI36 chr10: 108,940,848-120,510,991	RBM20, CCDC186, 147 more genes
nsv3905499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 104,030,479-115,410,590 , GRCh38.p12 chr10: 102,270,722-113,650,831	RBM20, RPS15AP30, 156 more genes
nsv3916477	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 104,481,920-115,834,854 , GRCh37 chr10: 104,491,930-115,844,864 , GRCh38 chr10: 102,732,173-114,085,105	RBM20, XPNPEP1, 147 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	RBM20, LOC100419870, 2105 more genes
nsv3891157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558	RBM20, AGAP14P, 2097 more genes
nsv3902271	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639	RBM20, ANXA11, 2085 more genes
nsv3891958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414	RBM20, TUBB8, 2085 more genes
nsv7137211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639	RBM20, EXOC6, 1906 more genes
nsv3905489	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,283,493-135,427,143 , GRCh38.p12 chr10: 91,523,736-133,613,639	RBM20, LOC105378476, 688 more genes

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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

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Items: 1 to 20 of 39

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Number of Variants: 20

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