dbVar for Gene (Select 730811) - 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
nsv6137753	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr2: 2,281,453-2,420,148 , GRCh37.p13 chr2: 2,285,225-2,423,920	MYT1L, MYT1L-AS1
nsv5450307	copy number variation	1	nstd206	human		GRCh38 chr2: 2,319,392-2,319,503 , GRCh37.p13 chr2: 2,323,164-2,323,275	MYT1L-AS1, MYT1L
nsv5437131	copy number variation	1	nstd206	human		GRCh38 chr2: 2,319,337-2,319,428 , GRCh37.p13 chr2: 2,323,109-2,323,200	MYT1L, MYT1L-AS1
nsv4892022	copy number variation	1	nstd200	human		GRCh38 chr2: 2,324,752-2,325,042 , GRCh37.p13 chr2: 2,328,524-2,328,814	MYT1L, MYT1L-AS1
nsv4769947	copy number variation	1	nstd200	human		GRCh37 chr2: 2,328,524-2,328,814 , GRCh38.p12 chr2: 2,324,752-2,325,042	MYT1L-AS1, MYT1L
nsv4728621	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 2,074,335-3,934,366 , GRCh38.p12 chr2: 2,070,563-3,886,776	LOC105373389, MYT1L, 18 more genes
nsv4707525	copy number variation	1	nstd195	human		GRCh37 chr2: 2,263,001-2,719,951 , GRCh38.p12 chr2: 2,259,229-2,716,179	MYT1L, MYT1L-AS1, 2 more genes
nsv4674784	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 1,045,542-4,104,255 , GRCh38.p12 chr2: 1,049,856-4,056,664	LOC105373390, MYT1L-AS1, 27 more genes
nsv4674039	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 12,770-3,000,954 , GRCh38.p12 chr2: 12,770-2,997,182	LINC01115, LOC105373352, 31 more genes
nsv4466643	mobile element insertion	1	nstd166	human		GRCh37.p13 chr2: 2,322,525-2,322,525 , GRCh38.p12 chr2: 2,318,753-2,318,753	MYT1L, MYT1L-AS1
nsv4454966	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,770-7,502,796 , GRCh38.p12 chr2: 12,770-7,362,665	LINC01810, ADI1, 83 more genes
nsv4454221	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 2,164,149-2,396,499 , GRCh38.p12 chr2: 2,160,377-2,392,727	MYT1L, MYT1L-AS1
nsv4453225	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 12,770-2,832,894 , GRCh38.p12 chr2: 12,770-2,829,122	LOC105373359, LOC107985839, 29 more genes
nsv4452632	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 12,770-3,819,558 , GRCh38.p12 chr2: 12,770-3,771,968	LOC107985838, LOC100996637, 45 more genes
nsv4452002	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 2,033,726-2,832,894 , GRCh38.p12 chr2: 2,029,954-2,829,122	LOC105373389, MYT1L, 2 more genes
nsv4449985	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 12,770-2,348,876 , GRCh38.p12 chr2: 12,770-2,345,104	PXDN, TPO, 27 more genes
nsv4070543	copy number variation	1	nstd166	human		GRCh37.p13 chr2: 2,323,109-2,323,200 , GRCh38.p12 chr2: 2,319,337-2,319,428	MYT1L-AS1, MYT1L
nsv4067488	copy number variation	1	nstd166	human		GRCh37.p13 chr2: 1,506,119-2,325,715 , GRCh38.p12 chr2: 1,502,347-2,321,943	TPO, PXDN, 4 more genes
nsv3908677	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr2: 2,770-4,344,326 , GRCh37 chr2: 12,770-4,366,451 , GRCh38 chr2: 12,770-4,318,861	LINC01865, EIPR1, 50 more genes
nsv3908628	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 20,342-14,924,526 , GRCh37 chr2: 30,342-15,007,075 , GRCh38 chr2: 30,342-14,866,951	RPS7, RPL30P3, 198 more genes

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Number of Variants: 20

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 113

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Number of Variants: 20

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