smpd3[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
nsv3906976	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 68,395,161-68,442,906 , GRCh38.p12 chr16: 68,361,258-68,409,003	SMPD3, PRMT7
nsv4675201	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 65,669,673-70,180,183 , GRCh38.p12 chr16: 65,635,770-70,146,280	SMPD3, LOC100420066, 143 more genes
nsv7094684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 68,349,883-68,732,303 , GRCh38.p12 chr16: 68,315,980-68,698,400	SMPD3, LOC105371321, 8 more genes
nsv3906108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224	SMPD3, CKLF, 1882 more genes
nsv3904593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973	SMPD3, LOC100128079, 1879 more genes
nsv3901410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287	SMPD3, LINC02175, 1877 more genes
nsv3909417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867	SMPD3, PRSS53, 1868 more genes
nsv3892266	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654	SMPD3, FTLP14, 1868 more genes
nsv3921269	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345	SMPD3, LOC105371237, 985 more genes
nsv6314755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654	SMPD3, ATMIN, 826 more genes
nsv3915506	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 51,490,596-88,682,563 , GRCh38 chr16: 52,899,183-90,088,654 , GRCh37 chr16: 52,933,095-90,155,062	SMPD3, CFAP69P1, 716 more genes
nsv3891306	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 57,051,473-89,797,669 , GRCh38.p12 chr16: 57,017,561-89,731,261	SMPD3, LOC107984894, 613 more genes
nsv3913913	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 62,980,782-88,675,894 , GRCh38 chr16: 64,389,378-90,081,985 , GRCh37 chr16: 64,423,281-90,148,393	SMPD3, ATP5F1AP3, 534 more genes
nsv3919817	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 63,904,799-88,675,894 , GRCh37 chr16: 65,347,298-90,148,393 , GRCh38 chr16: 65,313,395-90,081,985	SMPD3, LOC105376772, 527 more genes
nsv3910304	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 64,102,887-88,690,904 , GRCh38 chr16: 65,511,483-90,096,995 , GRCh37 chr16: 65,545,386-90,163,403	SMPD3, MC1R, 528 more genes
nsv3920399	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 61,517,334-83,176,902 , GRCh37 chr16: 62,959,833-84,619,401 , GRCh38 chr16: 62,925,929-84,585,795	SMPD3, LOC654780, 385 more genes
nsv3918521	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 48,276,933-66,993,116 , GRCh37 chr16: 49,719,432-68,435,615 , GRCh38 chr16: 49,685,521-68,401,712	SMPD3, CYLD-AS2, 342 more genes
nsv3893486	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 54,416,050-72,453,266 , GRCh38.p12 chr16: 54,382,138-72,419,367	SMPD3, ZNF19, 375 more genes
nsv3917492	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 64,549,233-82,202,549 , GRCh38 chr16: 65,957,829-83,611,443 , GRCh37 chr16: 65,991,732-83,645,048	SMPD3, ELMO3, 346 more genes
nsv3916321	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 58,490,026-74,742,621 , GRCh38 chr16: 58,456,122-74,708,723 , NCBI36 chr16: 57,047,527-73,300,122	SMPD3, RN7SL143P, 292 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 41

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Number of Variants: 20

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Supplemental Content

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