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

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6310640	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 47,109,064-47,112,410 , GRCh38.p12 chr19: 46,605,807-46,609,153	PTGIR, CALM3
nsv3891669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 43,013,365-47,241,534 , GRCh38.p12 chr19: 42,509,213-46,738,277	PTGIR, MIR320E, 189 more genes
nsv3910109	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 46,458,122-47,683,579 , GRCh37 chr19: 46,961,379-48,186,836 , NCBI36 chr19: 51,653,219-52,878,648	PTGIR, FKRP, 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	PTGIR, 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	PTGIR, 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	PTGIR, LENG8, 2408 more genes
nsv4457372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575	PTGIR, ZNF461, 735 more genes
nsv4676357	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308	PTGIR, MIR4324, 485 more genes
nsv3924836	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 50,166,517-53,452,471 , GRCh37 chr19: 45,474,677-48,760,659 , GRCh38 chr19: 44,971,420-48,257,402	PTGIR, IGFL1P1, 145 more genes
nsv4350827	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 47,036,361-48,525,536 , GRCh38.p12 chr19: 46,533,104-48,022,279	PTGIR, LINC01595, 59 more genes
nsv3900160	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 46,404,248-48,488,721 , GRCh38.p12 chr19: 45,900,990-47,985,464	PTGIR, C5AR1, 84 more genes
nsv3921787	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr19: 50,582,487-52,026,097 , GRCh37 chr19: 45,890,647-47,334,257 , GRCh38 chr19: 45,387,389-46,831,000	PTGIR, CALM3, 71 more genes
nsv7137151	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 47,028,919-48,185,409 , GRCh38.p12 chr19: 46,525,662-47,682,152	PTGIR, C5AR1, 36 more genes
nsv4676350	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 45,531,056-48,174,177 , GRCh38.p12 chr19: 45,027,798-47,670,920	PTGIR, NKPD1, 112 more genes
nsv3900603	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 46,918,881-47,782,258 , GRCh38.p12 chr19: 46,415,624-47,279,001	PTGIR, SAE1, 27 more genes
nsv3920398	copy number variation	2	nstd102	human	Uncertain significance	NCBI36 chr19: 51,629,587-52,026,097 , GRCh37 chr19: 46,937,747-47,334,257 , GRCh38 chr19: 46,434,490-46,831,000	PTGIR, LOC107987269, 16 more genes
nsv6310639	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 47,104,692-47,260,195 , GRCh38.p12 chr19: 46,601,435-46,756,938	PTGIR, PRKD2, 10 more genes
nsv4682791	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 47,109,074-47,260,205 , GRCh38.p12 chr19: 46,605,817-46,756,948	PTGIR, DACT3, 9 more genes

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