kynu[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
nsv4716485	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 143,634,577-143,719,262 , GRCh38 chr2: 142,877,008-142,961,693	KYNU, STIP1P1, 1 more genes
nsv6313475	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 143,440,277-143,686,832 , GRCh38.p12 chr2: 142,682,708-142,929,263	KYNU, LOC105373652, 2 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	KYNU, 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	KYNU, RNU6-675P, 300 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	KYNU, SPOPL-DT, 80 more genes
nsv6313481	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 143,258,712-152,867,819 , GRCh38.p12 chr2: 142,501,143-152,011,305	KYNU, STIP1P1, 98 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	KYNU, LOC105373651, 75 more genes
nsv3896212	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 140,186,521-146,528,244 , GRCh37 chr2: 140,944,090-147,285,812 , NCBI36 chr2: 140,660,560-147,002,282	KYNU, LOC101928361, 49 more genes
nsv3906959	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 142,140,576-148,319,701 , GRCh38 chr2: 141,666,537-147,845,662 , GRCh37 chr2: 142,424,106-148,603,231	KYNU, MTND6P11, 49 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	KYNU, 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	KYNU, 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	KYNU, 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	KYNU, 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	KYNU, 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	KYNU, 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	KYNU, YY1P2, 156 more genes
nsv6290982	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 142,409,401-152,680,804 , GRCh38.p12 chr2: 141,651,832-151,824,290	KYNU, LOC101928526, 101 more genes
nsv3885657	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 140,621,941-149,324,662 , GRCh38.p12 chr2: 139,864,372-148,567,093	KYNU, LOC101928386, 68 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	KYNU, ACTG2, 1713 more genes
nsv3884398	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 138,578,298-144,874,187 , GRCh38.p12 chr2: 137,820,728-144,116,620	KYNU, HNMT, 58 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

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Items: 1 to 20 of 29

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Number of Variants: 20

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