Mir375[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
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	MIR375, DAZAP2P1, 2991 more genes
nsv6313668	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062	MIR375, LOC105373947, 357 more genes
nsv3873368	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 218,813,434-227,450,699 , GRCh38.p12 chr2: 217,948,711-226,585,983	MIR375, ARPC2, 163 more genes
nsv3881607	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 219,135,239-220,290,732 , GRCh38.p12 chr2: 218,270,516-219,426,010	MIR375, BCS1L, 66 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	MIR375, 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	MIR375, 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	MIR375, 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	MIR375, MTND2P22, 3724 more genes
nsv4728725	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306	MIR375, LOC105376755, 1013 more genes
nsv3890898	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 188,818,195-242,065,208 , NCBI36 chr2: 189,391,166-242,656,032 , GRCh37 chr2: 189,682,921-243,007,359	MIR375, LOC105373909, 901 more genes
nsv3896499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 190,300,875-242,783,384 , NCBI36 chr2: 190,009,120-242,432,057 , GRCh38 chr2: 189,436,149-241,841,232	MIR375, RNU6-1206P, 883 more genes
nsv3908112	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 190,310,736-241,892,770 , NCBI36 chr2: 190,883,707-242,483,594 , GRCh37 chr2: 191,175,462-242,834,921	MIR375, LOC101928084, 871 more genes
nsv3902143	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 180,513,793-224,302,848 , NCBI36 chr2: 181,086,765-224,875,809 , GRCh37 chr2: 181,378,520-225,167,565	MIR375, LINC00607, 644 more genes
nsv3892046	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 195,763,507-237,382,556 , NCBI36 chr2: 195,471,752-237,047,295 , GRCh38 chr2: 194,898,783-236,473,913	MIR375, NPM1P46, 706 more genes
nsv7148056	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393	MIR375, DNAJB1P1, 580 more genes
nsv4436532	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 188,926,928-225,298,653 , GRCh38.p12 chr2: 188,062,201-224,433,936	MIR375, MARS2, 575 more genes
nsv3892823	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 211,444,400-243,059,659 , GRCh38 chr2: 210,579,676-242,126,245 , NCBI36 chr2: 211,152,645-242,717,069	MIR375, RPL19P5, 567 more genes
nsv3871121	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 213,518,431-242,783,384 , GRCh38.p12 chr2: 212,653,707-241,841,232	MIR375, TWIST2, 544 more genes
nsv4435891	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 210,779,657-239,879,183 , GRCh38.p12 chr2: 209,914,933-238,957,487	MIR375, XRCC5, 494 more genes
nsv3894025	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 218,674,727-242,717,069 , GRCh37 chr2: 218,966,482-243,059,659 , GRCh38 chr2: 218,101,759-242,126,245	MIR375, DNAJB6P3, 483 more genes

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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 32

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Number of Variants: 20

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Supplemental Content

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