rbm15[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6313675	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309	RBM15, LINC01307, 320 more genes
nsv5381058	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855	RBM15, AMYP1, 320 more genes
nsv3893941	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 97,648,746-111,014,655 , GRCh37 chr1: 97,876,158-111,213,132 , GRCh38 chr1: 97,410,602-110,670,510	RBM15, RPSAP19, 196 more genes
nsv3901500	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 101,856,241-112,047,173 , GRCh38 chr1: 101,618,097-111,703,028 , GRCh37 chr1: 102,083,653-112,245,650	RBM15, CHIAP1, 171 more genes
nsv3920130	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 103,429,843-112,252,782 , GRCh37.p13 chr1: 103,657,255-112,451,259 , GRCh38.p12 chr1: 103,191,699-111,908,637	RBM15, LOC105378898, 166 more genes
nsv3901806	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 105,812,437-112,534,771 , GRCh38 chr1: 105,468,292-112,190,626 , GRCh37 chr1: 106,010,914-112,733,248	RBM15, LOC126987, 151 more genes
nsv7095739	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 108,679,275-111,674,176 , GRCh38.p12 chr1: 108,136,653-111,131,554	RBM15, RPL7L1P21, 90 more genes
nsv6310577	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 110,603,355-111,147,404 , GRCh38.p12 chr1: 110,060,733-110,604,782	RBM15, LOC105378899, 17 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	RBM15, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	RBM15, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	RBM15, RNU1-153P, 4887 more genes
nsv3882464	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 93,837,992-121,343,783 , GRCh38.p12 chr1: 93,372,435-121,601,985	RBM15, LINC02607, 513 more genes
nsv3884558	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 94,054,724-111,671,707 , GRCh38.p12 chr1: 93,589,167-111,129,085	RBM15, SLC25A24, 265 more genes
nsv3890331	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 104,669,629-120,321,801 , GRCh37 chr1: 104,868,106-120,471,049 , GRCh38 chr1: 104,325,484-119,977,655	RBM15, OR11I1P, 324 more genes
nsv3898188	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 110,100,775-118,994,350 , GRCh38 chr1: 109,756,630-118,650,204 , GRCh37 chr1: 110,299,252-119,192,827	RBM15, AP4B1-AS1, 198 more genes
nsv3875681	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr1: 103,175,204-111,410,059 , GRCh37.p13 chr1: 103,640,760-111,952,681	RBM15, ALX3, 146 more genes
nsv4436700	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr1: 107,779,092-111,199,205 , GRCh38.p12 chr1: 107,236,470-110,656,583	RBM15, ALX3, 89 more genes
nsv4453642	copy number variation	1	nstd102	human	not provided	GRCh37 chr1: 108,926,313-111,266,497 , GRCh38.p12 chr1: 108,383,691-110,723,875	RBM15, PSMA5, 79 more genes
nsv6636999	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 110,662,135-111,401,322 , GRCh38.p12 chr1: 110,119,513-110,858,700	RBM15, LOC105378898, 19 more genes

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rbm15[All Fields] AND 1[has_clinical] (20)
dbVar
Full text in PMC (nucleotide) for Gene (Select 109801) (13)
PMC
Genome Links for Gene (Select 2909) (1)
Genome
Homo sapiens
Homo sapiens

Genome
PPP2R5C protein phosphatase 2 regulatory subunit B'gamma [Homo sapiens]
PPP2R5C protein phosphatase 2 regulatory subunit B'gamma [Homo sapiens]
Gene ID:5527

Gene

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