slc22a15[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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	SLC22A15, AMYP1, 320 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	SLC22A15, 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	SLC22A15, 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	SLC22A15, 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	SLC22A15, LINC02607, 513 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	SLC22A15, OR11I1P, 324 more genes
nsv6313671	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 111,647,582-121,343,783 , GRCh38.p12 chr1: 111,104,960-121,601,985	SLC22A15, GAPDHP23, 243 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	SLC22A15, AP4B1-AS1, 198 more genes
nsv3902511	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 116,403,765-120,474,160 , GRCh38 chr1: 116,059,621-120,130,051 , GRCh37 chr1: 116,602,242-120,672,637	SLC22A15, LINC01779, 89 more genes
nsv3874911	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 116,510,863-116,863,975 , GRCh38.p12 chr1: 115,968,242-116,321,353	SLC22A15, MAB21L3, 5 more genes
nsv7095742	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 116,310,909-116,947,066 , GRCh38.p12 chr1: 115,768,288-116,404,444	SLC22A15, LOC105378918, 12 more genes
nsv3873640	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 116,065,879-116,693,221 , GRCh38.p12 chr1: 115,523,258-116,150,600	SLC22A15, CNOT7P2, 12 more genes

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