znf37a[All Fields] AND 1[has_clinical] - dbVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 19

loading data ...

Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3894356	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 38,410,108-38,524,476 , GRCh38.p12 chr10: 38,121,180-38,235,548	ZNF37A, LOC105376500, 1 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	ZNF37A, RNU7-12P, 1876 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	ZNF37A, LOC100419870, 2105 more genes
nsv3891157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558	ZNF37A, AGAP14P, 2097 more genes
nsv3902271	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639	ZNF37A, ANXA11, 2085 more genes
nsv3891958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414	ZNF37A, TUBB8, 2085 more genes
nsv7137211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639	ZNF37A, EXOC6, 1906 more genes
nsv3904390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594	ZNF37A, LINC00700, 806 more genes
nsv3914331	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 32,328,854-38,448,615 , GRCh38 chr10: 31,999,920-38,119,681 , GRCh37 chr10: 32,288,848-38,408,609	ZNF37A, CCNY, 87 more genes
nsv3972353	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 37,149,872-46,169,876 , GRCh38.p12 chr10: 36,860,944-45,674,428	ZNF37A, ALOX5, 132 more genes
nsv3920598	copy number variation	1	nstd102	human	Benign	NCBI36 chr10: 4,636,926-47,125,152 , GRCh38 chr10: 4,604,734-48,074,662 , GRCh37 chr10: 4,646,926-47,531,169	ZNF37A, LOC100420467, 709 more genes
nsv4675921	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 37,189,335-38,900,673 , GRCh38.p12 chr10: 36,900,407-38,607,542	ZNF37A, ZNF248, 38 more genes
nsv4676011	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 38,064,033-38,900,673 , GRCh38.p12 chr10: 37,775,105-38,607,542	ZNF37A, EIF3LP3, 20 more genes
nsv3918146	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr10: 38,321,521-39,092,250 , GRCh37.p13 chr10: 38,281,515-39,052,244 , GRCh38.p12 chr10: 37,992,587-38,759,113	ZNF37A, EIF3LP3, 19 more genes
nsv6290893	copy number variation	1	nstd102	human	not provided	GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579	ZNF37A, C1QL3, 774 more genes
nsv3895851	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 36,797,203-38,900,673 , GRCh38.p12 chr10: 36,508,275-38,607,542	ZNF37A, VN1R53P, 39 more genes
nsv6313948	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 37,697,888-38,677,334 , GRCh38.p12 chr10: 37,408,960-38,388,406	ZNF37A, MTND1P18, 21 more genes
nsv3912415	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr10: 38,052,840-38,766,476 , NCBI36 chr10: 38,381,774-39,099,613 , GRCh37 chr10: 38,341,768-39,059,607	ZNF37A, CCNYL4, 17 more genes
nsv3922318	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr10: 38,469,582-39,110,801 , GRCh37 chr10: 38,429,576-39,070,795 , GRCh38 chr10: 38,140,648-38,777,664	ZNF37A, ACTR3BP5, 14 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

znf37a[All Fields] AND 1[has_clinical] (20)
dbVar

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)