cdk7[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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	CDK7, MEGF10, 2080 more genes
nsv6313676	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 64,049,692-70,306,646 , GRCh38.p12 chr5: 64,753,865-71,010,819	CDK7, BCL9P1, 105 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	CDK7, LOC100419549, 67 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	CDK7, LOC105374618, 2499 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	CDK7, PCDHGC5, 2492 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	CDK7, SPEF2, 2490 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	CDK7, LINC02241, 878 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	CDK7, TRIM23, 215 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	CDK7, CCNB1, 47 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	CDK7, TRIM23, 125 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	CDK7, TRIM23, 124 more genes
nsv6291088	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 68,203,539-68,641,982 , GRCh38.p12 chr5: 68,907,712-69,346,155	CDK7, CFL1P5, 14 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	CDK7, RNU1-150P, 1757 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	CDK7, LOC105378993, 2492 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	CDK7, SMN1, 97 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	CDK7, SERF1B, 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	CDK7, LOC112267932, 22 more genes

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