s1pr2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3912242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 9,846,119-11,338,677 , GRCh38 chr19: 9,735,443-11,228,001 , NCBI36 chr19: 9,707,119-11,199,677	S1PR2, PPAN, 68 more genes
nsv3900924	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 10,286,133-11,040,457 , GRCh38.p12 chr19: 10,175,457-10,929,781	S1PR2, MIR4322, 38 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	S1PR2, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	S1PR2, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	S1PR2, LENG8, 2408 more genes
nsv3898900	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 9,678,768-14,853,426 , GRCh38.p12 chr19: 9,568,092-14,742,614	S1PR2, FBXL12, 253 more genes
nsv3920643	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 10,267,082-11,000,364 , NCBI36 chr19: 10,128,082-10,861,364 , GRCh38 chr19: 10,156,406-10,889,688	S1PR2, MIR4748, 36 more genes
nsv3920616	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227	S1PR2, ACP5, 236 more genes
nsv6291543	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 9,941,033-11,739,567 , GRCh38.p12 chr19: 9,830,357-11,628,752	S1PR2, KRI1, 88 more genes

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