nobox[All Fields] AND 1[has_clinical] - 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
nsv7097611	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 144,094,333-144,532,695 , GRCh38.p12 chr7: 144,397,240-144,835,602 , GRCh38.p12 chr7\|NW_018654715.1: 446,707-680,662	NOBOX, EEF1A1P10, 3 more genes
nsv7097487	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 144,094,333-144,463,064 , GRCh38.p12 chr7\|NW_018654715.1: 446,707-680,662 , GRCh38.p12 chr7: 144,397,240-144,765,971	NOBOX, PPIAP83, 3 more genes
nsv6312532	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 144,094,333-144,150,776 , GRCh38.p12 chr7: 144,397,240-144,453,683 , GRCh38.p12 chr7\|NW_018654715.1: 446,707-503,140	NOBOX, RNU6ATAC40P, 2 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	NOBOX, RNU6-438P, 2682 more genes
nsv4675615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620	NOBOX, ATG9B, 603 more genes
nsv3915633	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 134,002,121-158,077,335 , GRCh38 chr7: 134,666,829-158,591,882 , GRCh37 chr7: 134,351,581-158,384,574	NOBOX, MOXD2P, 561 more genes
nsv3897512	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 137,917,376-159,119,707 , GRCh38.p12 chr7: 138,232,630-159,327,017	NOBOX, LOC105375548, 520 more genes
nsv7097864	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959	NOBOX, FAM131B, 466 more genes
nsv3903590	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 140,133,025-158,982,771 , GRCh38.p12 chr7: 140,433,225-159,190,080	NOBOX, LOC105375597, 468 more genes
nsv3910344	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 140,754,198-159,307,523 , GRCh37 chr7: 140,453,998-159,100,212 , NCBI36 chr7: 140,100,467-158,792,973	NOBOX, LOC112268012, 461 more genes
nsv3905379	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 140,636,858-159,119,707 , GRCh38.p12 chr7: 140,937,058-159,327,017	NOBOX, AGAP3, 459 more genes
nsv3919772	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 141,307,130-158,821,317 , GRCh37 chr7: 142,528,609-159,128,556 , GRCh38 chr7: 141,960,861-159,335,866	NOBOX, LOC105375567, 429 more genes
nsv6636458	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643	NOBOX, TRBD2, 403 more genes
nsv3904188	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 141,938,235-159,126,310 , GRCh38.p12 chr7: 142,288,582-159,333,620	NOBOX, RBM33-DT, 423 more genes
nsv3915683	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 143,884,559-159,282,390 , GRCh37 chr7: 143,581,652-159,075,079 , NCBI36 chr7: 143,212,585-158,767,840	NOBOX, FASTK, 280 more genes
nsv3907788	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 143,839,360-159,138,663 , GRCh38.p12 chr7: 144,142,267-159,335,973	NOBOX, GIMAP1, 264 more genes
nsv3914137	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 134,702,438-148,504,492 , NCBI36 chr7: 134,352,978-148,135,425 , GRCh38 chr7: 135,017,687-148,807,400	NOBOX, FAM180A, 348 more genes
nsv6290262	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 133,848,099-145,814,115 , GRCh38.p12 chr7: 134,163,347-146,117,023	NOBOX, TRBJ2-7, 341 more genes
nsv3919052	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 143,884,559-152,674,271 , GRCh37 chr7: 143,581,652-152,371,356 , NCBI36 chr7: 143,212,585-152,002,289	NOBOX, OR2F2, 194 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	NOBOX, RNU6-565P, 2684 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 53

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Number of Variants: 20

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Search details

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