Pyridin-2-amine 1-oxide monohydrochloride - 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
nsv3892943	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 50,710,306-50,999,091 , GRCh37 chr2: 50,937,444-51,226,229 , NCBI36 chr2: 50,790,948-51,079,733	NRXN1
nsv3883853	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 50,964,034-51,227,294 , GRCh38.p12 chr2: 50,736,896-51,000,156	NRXN1
nsv6313646	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 50,980,691-51,236,988 , GRCh38.p12 chr2: 50,753,553-51,009,850	NRXN1
nsv6290474	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 51,002,884-51,257,328 , GRCh38.p12 chr2: 50,775,746-51,030,190	NRXN1
nsv3895914	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 50,754,975-50,999,091 , NCBI36 chr2: 50,835,617-51,079,733 , GRCh37 chr2: 50,982,113-51,226,229	NRXN1
nsv1398664	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 51,005,771-51,246,088 , GRCh38.p12 chr2: 50,778,633-51,018,950	NRXN1
nsv3888386	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 50,721,552-50,944,617 , GRCh37.p13 chr2: 50,948,690-51,171,755	NRXN1
nsv7096205	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,307,172-15,519,975 , GRCh38.p12 chr2: 15,167,048-15,379,851	NBAS
nsv4674734	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 51,003,258-51,209,822 , GRCh38.p12 chr2: 50,776,120-50,982,684	NRXN1
nsv6313742	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 51,027,613-51,216,518 , GRCh38.p12 chr2: 50,800,475-50,989,380	NRXN1
nsv5673297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 200,136,914-200,320,780 , GRCh38.p12 chr2: 199,272,191-199,456,057	SATB2
nsv3901338	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 51,088,055-51,257,067 , NCBI36 chr2: 50,941,559-51,110,571 , GRCh38 chr2: 50,860,917-51,029,929	NRXN1
nsv4674375	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 50,352,345-50,520,197 , GRCh38.p12 chr2: 50,125,207-50,293,059	NRXN1
nsv6290535	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 50,991,242-51,158,769 , GRCh38.p12 chr2: 50,764,104-50,931,631	NRXN1
nsv6636613	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 51,047,025-51,209,824 , GRCh38.p12 chr2: 50,819,887-50,982,686	NRXN1
nsv3877692	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 51,032,041-51,189,570 , GRCh38.p12 chr2: 50,804,903-50,962,432	NRXN1
nsv7096391	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 200,173,463-200,320,760 , GRCh38.p12 chr2: 199,308,740-199,456,037	SATB2
nsv3885178	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 145,110,888-145,255,210 , GRCh38.p12 chr2: 144,353,321-144,497,643	ZEB2
nsv3874447	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 51,113,043-51,257,100 , GRCh38.p12 chr2: 50,885,905-51,029,962	NRXN1
nsv3906312	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 50,851,255-50,995,129 , NCBI36 chr2: 50,931,897-51,075,771 , GRCh37 chr2: 51,078,393-51,222,267	NRXN1

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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 110411

Page of 5521

Number of Variants: 20

Page of 5521

Supplemental Content

Find related data

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