dbVar for Gene (Select 324) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7097498	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 112,151,175-112,151,300 , GRCh38.p12 chr5: 112,815,478-112,815,603	APC
nsv7097497	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,072,721-112,164,689 , GRCh38.p12 chr5: 112,737,024-112,828,992	RNU6-482P, CBX3P3, 1 more genes
nsv7097108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,162,795-112,164,679 , GRCh38.p12 chr5: 112,827,098-112,828,982	APC
nsv7097015	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr5: 112,173,240-112,179,823 , GRCh38.p12 chr5: 112,837,543-112,844,126	APC
nsv7097014	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,128,133-112,179,823 , GRCh38.p12 chr5: 112,792,436-112,844,126	APC
nsv7097013	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 112,090,588-112,137,090 , GRCh38.p12 chr5: 112,754,891-112,801,393	APC, CBX3P3, 1 more genes
nsv7097012	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,043,009-112,151,300 , GRCh38.p12 chr5: 112,707,312-112,815,603	RNU6-482P, CBX3P3, 1 more genes
nsv7096875	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 112,136,966-112,137,090 , GRCh38.p12 chr5: 112,801,269-112,801,393	APC
nsv7096874	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,115,546-112,179,823 , GRCh38.p12 chr5: 112,779,849-112,844,126	APC
nsv7096873	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 112,111,316-112,170,882 , GRCh38.p12 chr5: 112,775,619-112,835,185	CBX3P3, RNU6-482P, 1 more genes
nsv7096872	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,102,013-112,102,117 , GRCh38.p12 chr5: 112,766,316-112,766,420	APC
nsv7096871	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,043,009-112,111,444 , GRCh38.p12 chr5: 112,707,312-112,775,747	CBX3P3, APC
nsv7096747	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,154,653-112,179,823 , GRCh38.p12 chr5: 112,818,956-112,844,126	APC
nsv7096746	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 112,043,009-112,179,823 , GRCh38.p12 chr5: 112,707,312-112,844,126	APC, CBX3P3, 1 more genes
nsv7096745	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,043,009-112,090,742 , GRCh38.p12 chr5: 112,707,312-112,755,045	APC
nsv7093111	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,036,100-112,045,850 , GRCh38.p12 chr5: 112,700,403-112,710,153	APC
nsv7093069	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr5: 112,828,991-112,829,079 , GRCh37 chr5: 112,164,688-112,164,776	APC
nsv7054819	inversion	1	nstd229	human		GRCh38 chr5: 112,393,108-116,183,657 , GRCh37.p13 chr5: 111,728,805-115,519,354	SRP19, LINCADL, 53 more genes
nsv7054501	inversion	1	nstd229	human		GRCh38 chr5: 112,796,972-112,796,989 , GRCh37.p13 chr5: 112,132,669-112,132,686	APC
nsv7047000	inversion	1	nstd229	human		GRCh38 chr5: 112,427,651-114,848,458 , GRCh37.p13 chr5: 111,763,348-114,184,155	XBP1P1, SRP19, 23 more genes

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Number of Variants: 20

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Items: 1 to 20 of 607

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Number of Variants: 20

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