mindy4b[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
nsv3915058	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 150,607,390-150,860,207 , NCBI36 chr3: 152,090,080-152,342,897 , GRCh38 chr3: 150,889,603-151,142,420	MINDY4B, MED12L, 2 more genes
nsv6636735	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 150,534,296-150,908,849 , GRCh38.p12 chr3: 150,816,509-151,191,062	MINDY4B, MED12L, 3 more genes
nsv6636766	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 150,546,825-150,878,912 , GRCh38.p12 chr3: 150,829,038-151,161,125	MINDY4B, MED12L, 2 more genes
nsv6290244	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334	MINDY4B, LOC102724145, 273 more genes
nsv3887637	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 148,425,748-153,220,169 , GRCh38.p12 chr3: 148,707,961-153,502,380	MINDY4B, LOC101927942, 97 more genes
nsv4674301	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 149,404,255-152,786,331 , GRCh38.p12 chr3: 149,686,468-153,068,542	MINDY4B, EIF3JP2, 63 more genes
nsv6311444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 148,447,967-151,176,497 , GRCh38.p12 chr3: 148,730,180-151,458,709	MINDY4B, TM4SF1, 68 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	MINDY4B, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	MINDY4B, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	MINDY4B, RPL23AP49, 2875 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	MINDY4B, LINC02614, 1469 more genes
nsv6637156	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502	MINDY4B, H1-10, 846 more genes
nsv3918692	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833	MINDY4B, LOC105374179, 785 more genes
nsv3874894	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 142,995,020-192,997,215 , GRCh38.p12 chr3: 143,276,178-193,279,426	MINDY4B, RNU6-901P, 673 more genes
nsv3918784	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 147,160,353-178,240,319 , GRCh38 chr3: 147,442,566-178,522,531 , NCBI36 chr3: 148,643,043-179,723,013	MINDY4B, LOC105374167, 394 more genes
nsv5381765	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911	MINDY4B, MBNL1-AS1, 339 more genes
nsv4684209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822	MINDY4B, MTAPP1, 339 more genes
nsv6290273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295	MINDY4B, LINC02066, 206 more genes
nsv6313678	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046	MINDY4B, RNU6-901P, 229 more genes
nsv3878556	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 150,352,753-153,522,663 , GRCh38.p12 chr3: 150,634,966-153,804,874	MINDY4B, AADAC, 45 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 22

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Number of Variants: 20

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Supplemental Content

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Search details

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