med7[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
nsv3911648	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 156,418,631-156,637,434 , GRCh38 chr5: 156,991,620-157,210,423 , NCBI36 chr5: 156,351,209-156,570,012	MED7, GARIN3, 3 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	MED7, MEGF10, 2080 more genes
nsv3886151	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 154,886,174-169,757,448 , GRCh38.p12 chr5: 155,506,614-170,330,444	MED7, CCNG1, 148 more genes
nsv3922783	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 152,761,187-167,248,053 , NCBI36 chr5: 152,120,940-166,607,636 , GRCh37 chr5: 152,140,747-166,675,058	MED7, APOOP1, 151 more genes
nsv3915958	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 152,443,869-166,104,392 , NCBI36 chr5: 151,803,623-165,463,975 , GRCh37 chr5: 151,823,430-165,531,397	MED7, C5orf52, 147 more genes
nsv4674945	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 156,347,980-169,959,880 , GRCh38.p12 chr5: 156,920,969-170,532,876	MED7, LINC02227, 146 more genes
nsv7096762	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr5: 155,338,082-156,899,968 , GRCh38.p12 chr5: 155,911,072-157,472,960	MED7, NIPAL4, 14 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	MED7, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	MED7, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	MED7, SPEF2, 2490 more genes
nsv3874238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337	MED7, PJA2, 1228 more genes
nsv6315448	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788	MED7, GRM6, 554 more genes
nsv3921182	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 149,094,155-180,699,152 , GRCh38 chr5: 149,714,592-181,272,151 , NCBI36 chr5: 149,074,348-180,631,758	MED7, RN7SKP148, 553 more genes
nsv3878636	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,125,085-157,574,910 , GRCh38.p12 chr5: 130,789,392-158,147,902	MED7, LOC100288484, 551 more genes
nsv3885523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 155,344,802-180,693,344 , GRCh38.p12 chr5: 155,917,792-181,266,343	MED7, WWC1, 446 more genes
nsv3924400	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 156,185,101-180,629,412 , GRCh37 chr5: 156,252,523-180,696,806 , GRCh38 chr5: 156,825,512-181,269,805	MED7, CEP192P1, 443 more genes
nsv6636891	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790	MED7, EFCAB9, 287 more genes
nsv3914878	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 146,520,648-163,194,778 , GRCh37.p13 chr5: 146,540,455-163,262,200 , GRCh38.p12 chr5: 147,160,892-163,835,194	MED7, LOC105378231, 247 more genes
nsv3884275	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 94,844,077-178,830,410 , GRCh38.p12 chr5: 95,508,373-179,403,409	MED7, LOC107986368, 1258 more genes
nsv6290966	copy number variation	1	nstd102	human	not provided	GRCh37 chr5: 155,970,607-162,450,579 , GRCh38.p12 chr5: 156,543,597-163,023,573	MED7, C1QTNF2, 86 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 24

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Number of Variants: 20

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Supplemental Content

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