prr36[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7095726	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 6,361,586-8,212,364 , GRCh38.p12 chr19: 6,361,575-8,147,480	PRR36, SLC25A23, 77 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	PRR36, 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	PRR36, 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	PRR36, LENG8, 2408 more genes
nsv3914351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555	PRR36, SEMA6B, 299 more genes
nsv3890584	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144	PRR36, PCP2, 250 more genes
nsv3911630	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr19: 7,787,972-7,948,153 , GRCh38 chr19: 7,723,086-7,883,268 , NCBI36 chr19: 7,693,972-7,854,153	PRR36, CLEC4M, 9 more genes
nsv7095676	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 7,586,521-8,670,595 , GRCh38.p12 chr19: 7,521,635-8,605,710	PRR36, LRRC8E, 53 more genes
nsv4676269	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 7,657,490-8,569,762 , GRCh38.p12 chr19: 7,592,604-8,504,878	PRR36, LRRC8E, 47 more genes
nsv4682037	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 7,587,617-8,373,194 , GRCh38.p12 chr19: 7,522,731-8,308,310	PRR36, XAB2, 40 more genes

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