dmxl2[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
nsv7094297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 51,755,556-51,773,840 , GRCh38.p12 chr15: 51,463,359-51,481,643	DMXL2
nsv7094720	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 51,745,727-51,745,858 , GRCh38.p12 chr15: 51,453,530-51,453,661	DMXL2
nsv7093608	insertion	1	nstd102	human	Pathogenic	GRCh37 chr15: 51,829,782-51,829,782 , GRCh38 chr15: 51,537,585-51,537,585	DMXL2
nsv7094298	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 51,837,760-51,839,625 , GRCh38.p12 chr15: 51,545,563-51,547,428	DMXL2
nsv4455142	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 51,708,028-51,874,928 , GRCh38.p12 chr15: 51,415,831-51,582,731	DMXL2
nsv4456341	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 51,717,028-51,792,612 , GRCh38.p12 chr15: 51,424,831-51,500,415	DMXL2
nsv7094719	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 51,741,181-51,792,448 , GRCh38.p12 chr15: 51,448,984-51,500,251	DMXL2
nsv7094546	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 51,741,181-51,787,351 , GRCh38.p12 chr15: 51,448,984-51,495,154	DMXL2
nsv3913810	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 49,571,258-49,593,986 , GRCh37.p13 chr15: 51,783,966-51,806,694 , GRCh38.p12 chr15: 51,491,769-51,514,497	DMXL2
nsv7094721	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 51,745,727-51,914,742 , GRCh38.p12 chr15: 51,453,530-51,622,545	DMXL2, LOC105370816
nsv7094386	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 51,687,012-51,748,586 , GRCh38.p12 chr15: 51,394,815-51,456,389	DMXL2, GLDN
nsv7094722	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 51,856,302-51,914,742 , GRCh38.p12 chr15: 51,564,105-51,622,545	DMXL2, LOC105370816
nsv3898808	copy number variation	1	nstd102	human	not provided	GRCh37 chr15: 51,673,125-51,942,596 , GRCh38.p12 chr15: 51,380,928-51,650,399	DMXL2, GLDN, 1 more genes
nsv4675172	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 51,630,691-51,891,698 , GRCh38.p12 chr15: 51,338,494-51,599,501	DMXL2, GLDN, 1 more genes
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	DMXL2, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	DMXL2, RNU6-18P, 1442 more genes
nsv3903255	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 41,689,327-52,446,981 , GRCh38.p12 chr15: 41,397,129-52,154,784	DMXL2, RN7SKP101, 234 more genes
nsv3903669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 43,759,773-53,252,240 , GRCh38.p12 chr15: 43,467,575-52,960,043	DMXL2, MIR4712, 188 more genes
nsv6313917	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 47,635,238-56,509,908 , GRCh38.p12 chr15: 47,343,041-56,217,710	DMXL2, PYGO1, 125 more genes
nsv3913164	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 50,864,913-59,646,577 , GRCh37 chr15: 51,157,110-59,938,776 , NCBI36 chr15: 48,944,402-57,726,068	DMXL2, LOC112268148, 131 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 46

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Number of Variants: 20

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