dbVar for Gene (Select 55212) - 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
nsv7137782	insertion	1	nstd232	human		GRCh37.p13 chr4: 122,782,834-122,782,834 , GRCh38.p12 chr4: 121,861,679-121,861,679	BBS7
nsv7096974	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 121,616,266-124,323,706 , GRCh38.p12 chr4: 120,695,111-123,402,551	RN7SL335P, QRFPR, 40 more genes
nsv7046043	inversion	1	nstd229	human		GRCh38 chr4: 121,571,489-125,148,298 , GRCh37.p13 chr4: 122,492,644-126,069,453	TRC-GCA2-1, LINC02435, 39 more genes
nsv7043432	inversion	1	nstd229	human		GRCh38 chr4: 117,041,189-125,064,058 , GRCh37.p13 chr4: 117,962,345-125,985,213	SEPTIN14P4, LINC02516, 109 more genes
nsv6750747	copy number variation	1	nstd229	human		GRCh38 chr4: 121,855,875-121,855,916 , GRCh37.p13 chr4: 122,777,030-122,777,071	BBS7
nsv6741047	copy number variation	1	nstd229	human		GRCh38 chr4: 121,655,546-121,871,460 , GRCh37.p13 chr4: 122,576,701-122,792,615	SMIM43, BBS7, 4 more genes
nsv6739749	copy number variation	1	nstd229	human		GRCh38 chr4: 121,865,101-121,878,000 , GRCh37.p13 chr4: 122,786,256-122,799,155	TRPC3, BBS7
nsv6739735	copy number variation	1	nstd229	human		GRCh38 chr4: 121,745,676-122,710,918 , GRCh37.p13 chr4: 122,666,831-123,632,073	CCNA2, TRPC3, 13 more genes
nsv6739486	copy number variation	1	nstd229	human		GRCh38 chr4: 121,838,762-121,842,120 , GRCh37.p13 chr4: 122,759,917-122,763,275	BBS7
nsv6570561	inversion	1	nstd223	human		GRCh38 chr4: 117,041,188-125,064,052 , GRCh37.p13 chr4: 117,962,344-125,985,207	MYOZ2, NT5C3AP1, 109 more genes
nsv6567037	inversion	1	nstd223	human		GRCh38 chr4: 121,856,575-121,856,887 , GRCh37.p13 chr4: 122,777,730-122,778,042	BBS7
nsv6564636	inversion	1	nstd223	human		GRCh38 chr4: 121,837,017-121,837,855 , GRCh37.p13 chr4: 122,758,172-122,759,010	BBS7
nsv6558478	inversion	1	nstd223	human		GRCh38 chr4: 121,829,406-121,830,194 , GRCh37.p13 chr4: 122,750,561-122,751,349	BBS7
nsv6382275	copy number variation	1	nstd223	human		GRCh38 chr4: 121,625,271-122,343,784 , GRCh37.p13 chr4: 122,546,426-123,264,939	LOC112268469, CCNA2, 10 more genes
nsv6376905	copy number variation	1	nstd223	human		GRCh38 chr4: 121,859,301-121,860,300 , GRCh37.p13 chr4: 122,780,456-122,781,455	BBS7
nsv6376807	copy number variation	1	nstd223	human		GRCh38 chr4: 121,852,041-121,852,767 , GRCh37.p13 chr4: 122,773,196-122,773,922	BBS7
nsv6315092	insertion	1	nstd102	human	Uncertain significance	GRCh38 chr4: 121,822,648-121,822,648 , GRCh37 chr4: 122,743,803-122,743,803	CCNA2, BBS7
nsv6313878	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443	LINC00613, GYPA, 448 more genes
nsv6313750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 116,888,785-129,649,979 , GRCh38.p12 chr4: 115,967,629-128,728,824	LOC105377395, SEPTIN7P14, 152 more genes
nsv6291432	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354	SNHG27, TNIP3, 1091 more genes

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Number of Variants: 20

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