ctso[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
nsv6310588	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 150,776,487-150,779,291 , GRCh38.p12 chr1: 150,804,011-150,806,815	CTSK
nsv6310589	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr1: 150,778,175-150,778,629 , GRCh38.p12 chr1: 150,805,699-150,806,153	CTSK
nsv6310522	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 150,769,275-150,772,205 , GRCh38.p12 chr1: 150,796,799-150,799,729	UBE2D3P3, CTSK
nsv4728565	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 150,687,807-150,775,422 , GRCh38.p12 chr1: 150,715,331-150,802,946	CTSK, UBE2D3P3, 3 more genes
nsv3912840	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	CRB1, STX6, 1608 more genes
nsv3919458	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 155,162,982-170,959,553 , GRCh37 chr4: 156,084,134-171,880,704 , NCBI36 chr4: 156,303,584-172,117,279	CTSO, AIDAP2, 172 more genes
nsv3874224	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 153,203,431-162,912,359 , GRCh38.p12 chr4: 152,282,279-161,991,207	CTSO, PLRG1, 120 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	MARK1, LINC02766, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	SNAP47, STK40, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	RNU1-153P, MIR3917, 4887 more genes
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	CTSO, LOC100422029, 2358 more genes
nsv3876533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611	CTSO, LOC100420289, 2347 more genes
nsv3884499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286	CTSO, MTND4LP29, 2341 more genes
nsv3880085	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318	CTSO, LOC112268460, 2345 more genes
nsv3883791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495	CTSO, LOC105377343, 2341 more genes
nsv3875534	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 93,071,152-190,957,473 , GRCh38.p12 chr4: 92,150,001-190,036,318	CTSO, KLKB1, 1118 more genes
nsv3918947	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	LOC101060227, LINC01720, 1608 more genes
nsv3874596	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 109,199,664-189,752,726 , GRCh38.p12 chr4: 108,278,508-188,831,572	CTSO, RPL6P12, 938 more genes
nsv3924008	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 118,065,569-190,042,639 , GRCh37 chr4: 118,986,724-190,828,225 , NCBI36 chr4: 119,206,172-191,200,788	CTSO, PPID, 828 more genes
nsv3874610	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 119,437,495-190,904,301 , GRCh38.p12 chr4: 118,516,340-189,983,146	CTSO, OTUD4, 813 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 50

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Number of Variants: 20

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