me3[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
nsv3899439	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 86,282,680-86,306,401 , GRCh38.p12 chr11: 86,571,638-86,595,359	ME3
nsv3894049	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 86,282,680-86,286,290 , GRCh38.p12 chr11: 86,571,638-86,575,248	ME3
nsv4675643	copy number variation	2	nstd102	human	Uncertain significance, Likely benign	GRCh37 chr11: 86,217,857-86,429,093 , GRCh38.p12 chr11: 86,506,815-86,718,051	ME3, ME3-DT
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	MEGF10, LOC100128407, 2080 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	ME3, FAUP4, 2031 more genes
nsv3884357	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440	TXNDC15, PCDHAC1, 962 more genes
nsv3912937	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387	LINC01023, CTB-99A3.1, 783 more genes
nsv3904761	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514	ME3, RPS6P16, 449 more genes
nsv3913977	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356	ME3, PLS1P1, 349 more genes
nsv6637396	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313	ME3, LOC107984375, 295 more genes
nsv3921121	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688	ME3, LOC105369441, 296 more genes
nsv6313961	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717	ME3, MTND5P38, 252 more genes
nsv3922508	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 85,242,847-102,920,097 , GRCh37 chr11: 84,953,891-102,738,968 , NCBI36 chr11: 84,631,539-102,296,037	ME3, AMOTL1, 240 more genes
nsv3897292	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 80,318,996-96,116,221 , GRCh38.p12 chr11: 80,607,952-96,383,057	ME3, FAM181B, 218 more genes
nsv3901209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 81,771,852-90,851,187 , GRCh38.p12 chr11: 82,060,810-91,118,019	ME3, RPL7AP54, 124 more genes
nsv6637847	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 80,562,738-88,663,067 , GRCh38.p12 chr11: 80,851,695-88,929,899	ME3, PRSS23, 92 more genes
nsv3924309	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 138,206,826-145,191,872 , GRCh38 chr5: 138,871,137-145,812,309 , NCBI36 chr5: 138,234,725-145,172,065	FCHSD1, LOC105378208, 183 more genes
nsv4674839	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 83,530,179-87,059,742 , GRCh38.p12 chr11: 83,819,136-87,348,700	ME3, PICALM, 44 more genes
nsv3877607	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 83,315,294-86,755,595 , GRCh38.p12 chr11: 83,604,251-87,044,553	ME3, OR7E13P, 43 more genes
nsv3872314	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 139,147,238-141,540,491 , GRCh38.p12 chr5: 139,767,653-142,160,926	VTRNA1-1, HDAC3, 122 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 55

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Number of Variants: 20

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