lmf1[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
nsv7094645	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,004,337-1,004,686 , GRCh38.p12 chr16: 954,337-954,686	LMF1
nsv7094951	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 960,911-961,099 , GRCh38.p12 chr16: 910,911-911,099	LMF1
nsv6310043	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 929,550-929,757 , GRCh38.p12 chr16: 879,550-879,757	LMF1
nsv3921349	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr16: 969,283-995,770 , GRCh38 chr16: 979,282-1,005,769 , GRCh37 chr16: 1,029,282-1,055,769	LMF1, SOX8, 1 more genes
nsv3901514	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 1,030,772-1,032,632 , GRCh38.p12 chr16: 980,772-982,632	LMF1, CEROX1, 1 more genes
nsv3909086	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 1,031,450-1,032,776 , GRCh38.p12 chr16: 981,450-982,776	LMF1, SOX8, 1 more genes
nsv3898226	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 1,031,450-1,032,632 , GRCh38.p12 chr16: 981,450-982,632	LMF1, SOX8, 1 more genes
nsv3922820	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr16: 1,029,282-1,035,951 , GRCh38 chr16: 979,282-985,951 , NCBI36 chr16: 969,283-975,952	LMF1, CEROX1, 1 more genes
nsv3909964	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 1,029,282-1,035,586 , GRCh38 chr16: 979,282-985,586 , NCBI36 chr16: 969,283-975,587	LMF1, SOX8, 1 more genes
nsv3892451	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 1,030,840-1,032,632 , GRCh38.p12 chr16: 980,840-982,632	LMF1, SOX8, 1 more genes
nsv4456286	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 852,397-988,759 , GRCh38.p12 chr16: 802,397-938,759	LMF1, PRR25, 2 more genes
nsv4455481	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 1,026,478-1,134,445 , GRCh38.p12 chr16: 976,478-1,084,445	LMF1, SSTR5-AS1, 3 more genes
nsv4455594	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-2,053,328 , GRCh38.p12 chr16: 35,880-2,003,327	LMF1, JPT2, 128 more genes
nsv3919589	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 36,766-1,987,584 , GRCh37 chr16: 96,766-2,047,583 , GRCh38 chr16: 46,766-1,997,582	LMF1, C1QTNF8, 127 more genes
nsv3914731	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 46,722-1,867,327 , NCBI36 chr16: 36,722-1,857,329 , GRCh37 chr16: 96,722-1,917,328	LMF1, TPSP2, 110 more genes
nsv3897602	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-1,875,694 , GRCh38.p12 chr16: 35,880-1,825,693	LMF1, CHTF18, 110 more genes
nsv3919625	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 23,141-1,773,349 , NCBI36 chr16: 13,141-1,763,351 , GRCh37 chr16: 73,141-1,823,350	LMF1, RHOT2, 106 more genes
nsv3916129	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 13,141-1,702,525 , GRCh38 chr16: 23,141-1,712,523 , GRCh37 chr16: 73,141-1,762,524	LMF1, C4orf46P1, 102 more genes
nsv3906615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-1,715,454 , GRCh38.p12 chr16: 38,165-1,665,453	LMF1, LOC105371046, 97 more genes
nsv3890088	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-1,593,645 , GRCh38.p12 chr16: 11,451-1,543,644	LMF1, CACNA1H, 100 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 77

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Number of Variants: 20

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