dbVar for Gene (Select 8507) - 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
nsv5560947	sequence alteration	1	nstd206	human		GRCh38 chr5: 74,581,386-75,393,871 , GRCh37.p13 chr5: 73,877,211-74,689,696	HEXB, GFM2, 18 more genes
nsv4937819	copy number variation	1	nstd200	human		GRCh38 chr5: 74,620,107-74,626,398 , GRCh37.p13 chr5: 73,915,932-73,922,223	ENC1
nsv4675667	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166	LOC101929380, LIX1-AS1, 318 more genes
nsv4675088	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 72,829,994-74,076,751 , GRCh38.p12 chr5: 73,534,169-74,780,926	NSA2, RNU7-196P, 17 more genes
nsv4436202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379	RNU1-150P, RNU6-727P, 1757 more genes
nsv4115271	copy number variation	1	nstd166	human		GRCh37.p13 chr5: 73,915,932-73,922,223 , GRCh38.p12 chr5: 74,620,107-74,626,398	ENC1
nsv3917856	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 74,163,186-110,809,453 , NCBI36 chr5: 73,494,767-110,173,052 , GRCh37 chr5: 73,459,011-110,145,153	CSNK1A1P3, POLR3G, 413 more genes
nsv3912593	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259	LOC105378993, LOC107986375, 2492 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	MEGF10, LOC100128407, 2080 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	LOC105374618, HARS1, 2499 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	SPEF2, NDST1, 2490 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	PCDHGC5, RGS14, 2492 more genes
nsv3136609	copy number variation	1	nstd151	human		GRCh37 chr5: 73,930,538-74,137,506 , GRCh38.p12 chr5: 74,634,713-74,841,681	NSA2, HEXB, 6 more genes
nsv3124337	copy number variation	1	nstd151	human		GRCh37 chr5: 73,930,538-74,065,194 , GRCh38.p12 chr5: 74,634,713-74,769,369	GFM2, NSA2, 3 more genes
nsv2343908	short tandem repeat	4	nstd128	human		GRCh37 chr5: 73,932,552-73,932,567 , GRCh38.p12 chr5: 74,636,727-74,636,742	ENC1
nsv2342523	short tandem repeat	1	nstd128	human		GRCh37 chr5: 73,936,668-73,936,710 , GRCh38.p12 chr5: 74,640,843-74,640,885	ENC1, HEXB
nsv2342389	short tandem repeat	11	nstd128	human		GRCh37 chr5: 73,933,581-73,933,618 , GRCh38.p12 chr5: 74,637,756-74,637,793	ENC1
nsv2342388	short tandem repeat	1	nstd128	human		GRCh37 chr5: 73,930,238-73,930,262 , GRCh38.p12 chr5: 74,634,413-74,634,437	ENC1
nsv2342387	short tandem repeat	2	nstd128	human		GRCh37 chr5: 73,927,007-73,927,028 , GRCh38.p12 chr5: 74,631,182-74,631,203	ENC1
nsv2342386	short tandem repeat	2	nstd128	human		GRCh37 chr5: 73,926,990-73,927,000 , GRCh38.p12 chr5: 74,631,165-74,631,175	ENC1

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Number of Variants: 20

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