dbVar for Gene (Select 6880) - 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
nsv5888268	copy number variation	1	nstd209	human		GRCh38 chr5: 69,366,792-69,367,355 , GRCh37.p13 chr5: 68,662,619-68,663,182	RAD17, TAF9, 1 more genes
nsv4593213	copy number variation	1	nstd183	human		GRCh37 chr5: 68,664,883-68,667,150 , GRCh38.p12 chr5\|NW_003315917.2: 152,252-154,519 , GRCh38.p12 chr5: 69,369,056-69,371,323	RAD17, TAF9, 1 more genes
nsv4578696	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr5: 58,780,641-73,523,380 , GRCh37.p13 chr5: 58,076,468-72,819,205	TRIM23, BTF3, 215 more genes
nsv4495273	mobile element insertion	1	nstd166	human		GRCh37.p13 chr5: 68,659,248-68,659,248 , GRCh38.p12 chr5\|NW_003315917.2: 146,616-146,616 , GRCh38.p12 chr5: 69,363,421-69,363,421	TAF9, AK6
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
nsv3960535	insertion	1	nstd168	human		GRCh38 chr5: 69,075,501-69,696,302 , GRCh37.p13 chr5: 68,371,328-68,992,129	CDK7, TAF9, 25 more genes
nsv3921568	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 64,228,590-68,791,331 , NCBI36 chr5: 64,264,346-68,827,087 , GRCh38 chr5: 64,932,763-69,495,504	LOC100419549, MAST4-AS1, 67 more genes
nsv3920547	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr5: 65,976,124-71,317,474 , NCBI36 chr5: 65,307,708-70,649,057 , GRCh37 chr5: 65,271,952-70,613,301	SMN1, NAIP, 97 more genes
nsv3920421	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr5: 62,538,695-70,622,774 , GRCh37 chr5: 62,502,939-70,587,018 , GRCh38 chr5: 63,207,112-71,291,191	TRIM23, CCNB1, 124 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
nsv3911585	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550	LINC02241, ATPSCKMT, 878 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
nsv3883692	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 58,966,132-68,847,066 , GRCh38.p12 chr5: 59,670,306-69,551,239	TRIM23, CCNB1, 125 more genes
nsv3883673	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 68,247,522-70,657,688 , GRCh38.p12 chr5\|NW_003315917.2: 1-1,360,365 , GRCh38.p12 chr5: 68,951,695-71,361,861	SERF1B, LOC105369228, 77 more genes
nsv3882001	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 68,313,021-68,847,066 , GRCh38.p12 chr5: 69,017,194-69,551,239 , GRCh38.p12 chr5\|NW_003315917.2: 1-334,184	LOC112267932, LOC100130639, 22 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
nsv3875076	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 65,315,606-68,755,816 , GRCh38.p12 chr5: 66,019,778-69,459,989	CCNB1, CDK7, 47 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
nsv3137876	copy number variation	1	nstd151	human		GRCh37 chr5: 68,647,885-68,728,925 , GRCh38.p12 chr5\|NW_003315917.2: 135,251-216,079 , GRCh38.p12 chr5: 69,352,058-69,433,098	AK6, RAD17, 2 more genes

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Number of Variants: 20

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