hnmt[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
nsv3884066	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 138,323,267-138,763,330 , GRCh38.p12 chr2: 137,565,697-138,005,760	HNMT, LOC101928273, 2 more genes
nsv4452653	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 138,319,338-138,787,042 , GRCh38.p12 chr2: 137,561,768-138,029,472	HNMT, LOC107985948, 2 more genes
nsv3913290	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr2: 138,330,381-138,625,008 , GRCh37.p13 chr2: 138,613,911-138,908,538 , GRCh38.p12 chr2: 137,856,341-138,150,968	HNMT, LOC107985948, 3 more genes
nsv4452687	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 138,673,890-138,792,148 , GRCh38.p12 chr2: 137,916,320-138,034,578	HNMT, LOC101928273, 1 more genes
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	HNMT, DAZAP2P1, 2991 more genes
nsv6290867	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 122,699,106-143,799,629 , GRCh38.p12 chr2: 121,941,530-143,042,060	HNMT, RNU6-675P, 300 more genes
nsv3876229	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 120,571,363-141,627,287 , GRCh38.p12 chr2: 119,813,787-140,869,718	HNMT, MIR9986, 320 more genes
nsv3897428	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 123,445,762-140,592,538 , NCBI36 chr2: 123,919,808-141,066,577 , GRCh37 chr2: 124,203,338-141,350,107	HNMT, ARHGAP42P2, 278 more genes
nsv3890186	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 136,937,358-146,681,810 , GRCh37 chr2: 137,694,928-147,439,378 , NCBI36 chr2: 137,411,398-147,155,848	HNMT, SPOPL-DT, 80 more genes
nsv4685664	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 137,639,637-146,827,604 , GRCh38.p12 chr2: 136,882,067-146,070,036	HNMT, LOC105373651, 75 more genes
nsv3910856	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 134,449,789-141,806,260 , GRCh37.p13 chr2: 134,733,319-142,089,790 , GRCh38.p12 chr2: 133,975,748-141,332,221	HNMT, LOC105373643, 73 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	HNMT, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	HNMT, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	HNMT, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	HNMT, MTND2P22, 3724 more genes
nsv6291353	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036	HNMT, LINC01120, 490 more genes
nsv6314748	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432	HNMT, MED15P9, 474 more genes
nsv5381338	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 136,473,383-152,727,396 , GRCh38.p12 chr2: 135,715,813-151,870,882	HNMT, YY1P2, 156 more genes
nsv3902350	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 136,045,480-142,845,159 , NCBI36 chr2: 136,519,520-143,319,198 , GRCh37 chr2: 136,803,050-143,602,728	HNMT, LOC101928273, 48 more genes
nsv6314726	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196	HNMT, ACTG2, 1713 more genes

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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 29

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Number of Variants: 20

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