cse1l[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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	CSE1L, PABPC1L, 170 more genes
nsv3908507	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 47,627,844-52,045,480 , GRCh38.p12 chr20: 49,011,307-53,428,941	CSE1L, LOC100419570, 93 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	CSE1L, 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	CSE1L, 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	CSE1L, 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	CSE1L, 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	CSE1L, 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	CSE1L, FTLP1, 472 more genes
nsv1398389	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 47,682,662-49,884,981 , GRCh38.p12 chr20: 49,066,125-51,268,444	CSE1L, CEBPB, 65 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	CSE1L, LOC107985439, 11 more genes
nsv4681865	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 47,538,407-48,099,037 , GRCh38.p12 chr20: 48,921,870-49,482,500	CSE1L, ARFGEF2, 12 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	CSE1L, 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	CSE1L, 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	CSE1L, PREX1, 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	CSE1L, ZFAS1, 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	CSE1L, ZNFX1, 13 more genes

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cse1l[All Fields] AND 1[has_clinical] (17)
dbVar
txid7227[Organism] (1154679)
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