prex1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3894314	copy number variation	1	nstd102	human	Benign	GRCh37 chr20: 47,308,798-47,536,334 , GRCh38.p12 chr20: 48,692,260-48,919,797	PREX1, ARFGEF2
nsv3890904	copy number variation	1	nstd102	human	Benign	GRCh37 chr20: 47,177,768-47,262,549 , GRCh38.p12 chr20: 48,561,230-48,646,011	PREX1, LOC105372646
nsv6290315	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 42,985,044-48,599,046 , GRCh38.p12 chr20: 44,356,404-49,982,509	PREX1, PABPC1L, 170 more genes
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	PREX1, TGIF2-RAB5IF, 1314 more genes
nsv3905072	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435	PREX1, LRRN4, 1313 more genes
nsv3895314	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202	PREX1, PKIG, 1311 more genes
nsv3896520	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110	PREX1, COMMD7, 1311 more genes
nsv3920218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118	PREX1, MIR3646, 1310 more genes
nsv3915005	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321	PREX1, FTLP1, 472 more genes
nsv3890266	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr20: 46,856,288-47,737,187 , GRCh38.p12 chr20: 48,227,545-49,120,650	PREX1, LOC107985439, 11 more genes
nsv3901847	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 46,874,875-47,442,163 , GRCh38.p12 chr20: 48,246,132-48,825,626	PREX1, LOC105372646, 6 more genes
nsv3910818	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167	PREX1, RNA5SP481, 855 more genes
nsv3874236	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 46,962,638-50,647,699 , GRCh38.p12 chr20: 48,333,895-52,031,160	PREX1, MIR645, 85 more genes
nsv6291599	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 46,721,299-47,873,110 , GRCh38.p12 chr20: 48,092,556-49,256,573	PREX1, STAU1, 16 more genes
nsv3920108	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 47,373,123-48,148,892 , NCBI36 chr20: 46,806,530-47,582,299 , GRCh38 chr20: 48,756,586-49,532,355	PREX1, ZFAS1, 14 more genes
nsv3899962	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 46,582,570-47,333,968 , GRCh38.p12 chr20: 47,953,826-48,717,430	PREX1, LOC107985439, 14 more genes
nsv3906682	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 47,427,610-48,085,774 , GRCh38.p12 chr20: 48,811,073-49,469,237	PREX1, ZNFX1, 13 more genes

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