adamts3[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
nsv4728967	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr4: 73,222,936-73,389,169 , GRCh38.p12 chr4: 72,357,219-72,523,452	ADAMTS3
nsv3921480	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr4: 73,647,634-73,913,117 , GRCh37.p13 chr4: 73,428,770-73,694,253 , GRCh38.p12 chr4: 72,563,053-72,828,536	ADAMTS3, HNRNPA1P67
nsv4674566	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 72,834,889-73,561,412 , GRCh38.p12 chr4: 71,969,172-72,695,695	ADAMTS3, NPFFR2
nsv4674172	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 73,184,648-73,813,059 , GRCh38.p12 chr4: 72,318,931-72,947,342	ADAMTS3, HNRNPA1P67
nsv3883055	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 73,184,648-73,812,869 , GRCh38.p12 chr4: 72,318,931-72,947,152	ADAMTS3, HNRNPA1P67
nsv3915924	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 73,160,675-73,549,259 , GRCh37.p13 chr4: 72,941,811-73,330,395 , GRCh38.p12 chr4: 72,076,094-72,464,678	ADAMTS3, NPFFR2
nsv6291252	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 72,998,352-73,320,894 , GRCh38.p12 chr4: 72,132,635-72,455,177	ADAMTS3, NPFFR2
nsv3923759	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502	ADAMTS3, EREG, 530 more genes
nsv5674237	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872	ADAMTS3, FTLP10, 335 more genes
nsv4729598	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,412,409-87,920,784 , GRCh38.p12 chr4: 70,546,692-86,999,632	ADAMTS3, PTPN11P5, 244 more genes
nsv6314916	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 67,833,055-82,716,065 , GRCh37.p13 chr4: 68,698,773-83,637,218	ADAMTS3, MICOS10P4, 274 more genes
nsv4674589	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 72,680,879-86,426,232 , GRCh38.p12 chr4: 71,815,162-85,505,079	ADAMTS3, SOWAHB, 211 more genes
nsv6313740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 61,867,555-74,711,517 , GRCh38.p12 chr4: 61,001,837-73,845,800	ADAMTS3, CXCL8, 175 more genes
nsv4674141	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,950,363-79,738,598 , GRCh38.p12 chr4: 68,084,645-78,817,444	ADAMTS3, COX18, 216 more genes
nsv3884502	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 66,017,575-76,772,947 , GRCh38.p12 chr4: 65,151,857-75,851,794	ADAMTS3, RNU2-40P, 188 more genes
nsv6313715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 73,055,313-80,083,154 , GRCh38.p12 chr4: 72,189,596-79,162,000	ADAMTS3, CCNG2, 129 more genes
nsv3913248	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 66,002,875-73,398,274 , GRCh38 chr4: 65,454,562-72,313,693 , GRCh37 chr4: 66,320,280-73,179,410	ADAMTS3, LOC105377262, 126 more genes
nsv4456138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,561,780-78,304,341 , GRCh38.p12 chr4: 70,696,063-77,383,187	ADAMTS3, ANKRD17-DT, 119 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	ADAMTS3, 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	ADAMTS3, LOC100420289, 2347 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 35

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Number of Variants: 20

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