lysmd3[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
nsv6290826	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 89,720,318-90,293,526 , GRCh38.p12 chr5: 90,424,501-90,997,709	LYSMD3, MBLAC2, 3 more genes
nsv3921192	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 89,559,719-90,448,165 , GRCh37 chr5: 89,523,963-90,412,409 , GRCh38 chr5: 90,228,146-91,116,592	LYSMD3, CETN3, 7 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	LYSMD3, MEGF10, 2080 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	LYSMD3, TXNDC15, 962 more genes
nsv3916468	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 89,670,423-127,412,115 , GRCh38 chr5: 90,374,606-128,076,423 , NCBI36 chr5: 89,706,179-127,440,014	LYSMD3, LOC105379149, 406 more genes
nsv3924896	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 84,603,580-111,435,081 , GRCh37 chr5: 83,899,398-110,770,779 , NCBI36 chr5: 83,935,154-110,798,678	LYSMD3, LOC107986438, 254 more genes
nsv3914008	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 88,377,169-104,022,949 , NCBI36 chr5: 88,412,925-104,050,848 , GRCh38 chr5: 89,081,352-104,687,248	LYSMD3, LOC105379080, 166 more genes
nsv3921368	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 86,672,700-100,860,147 , NCBI36 chr5: 86,708,456-100,888,046 , GRCh38 chr5: 87,376,883-101,524,443	LYSMD3, LOC107986438, 158 more genes
nsv6313788	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 82,185,951-90,110,454 , GRCh38.p12 chr5: 82,890,132-90,814,637	LYSMD3, RASA1, 82 more genes
nsv3874231	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 87,512,314-95,096,562 , GRCh38.p12 chr5: 88,216,497-95,760,858	LYSMD3, ARRDC3, 71 more genes
nsv7148188	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 88,189,536-93,784,597 , GRCh37.p13 chr5: 87,485,353-93,120,303	LYSMD3, RPS3AP22, 49 more genes
nsv3915072	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 86,743,723-92,337,264 , GRCh37 chr5: 86,039,540-91,633,081 , NCBI36 chr5: 86,075,296-91,668,837	LYSMD3, RAB5CP2, 54 more genes
nsv3922083	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 86,766,959-92,148,845 , GRCh37 chr5: 86,062,776-91,444,662 , NCBI36 chr5: 86,098,532-91,480,418	LYSMD3, LOC107986387, 52 more genes
nsv3916149	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 88,268,343-93,463,479 , GRCh38 chr5: 88,936,770-94,102,018 , GRCh37 chr5: 88,232,587-93,437,723	LYSMD3, MIR3660, 39 more genes
nsv3916966	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 87,664,106-91,698,938 , NCBI36 chr5: 87,699,862-91,724,694 , GRCh38 chr5: 88,368,289-92,363,231	LYSMD3, LOC107986433, 34 more genes
nsv3872102	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 87,764,485-90,147,447 , GRCh38.p12 chr5: 88,468,668-90,851,630	LYSMD3, LOC731157, 18 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	LYSMD3, 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	LYSMD3, 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	LYSMD3, SPEF2, 2490 more genes
nsv3917856	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 74,163,186-110,809,453 , NCBI36 chr5: 73,494,767-110,173,052 , GRCh37 chr5: 73,459,011-110,145,153	LYSMD3, CSNK1A1P3, 413 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

Find related data

Search details

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