uts2[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
nsv4674688	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 7,840,942-8,007,922 , GRCh38.p12 chr1: 7,780,882-7,947,862	UTS2, PER3, 3 more genes
nsv6290672	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570	UTS2, RPL9P11, 466 more genes
nsv7098827	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749	UTS2, LOC107985467, 386 more genes
nsv3900501	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 3,006,193-17,688,934 , GRCh37 chr1: 2,922,757-18,015,429 , NCBI36 chr1: 2,912,617-17,888,016	UTS2, MFFP1, 364 more genes
nsv3873030	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 746,608-15,077,159 , GRCh38.p12 chr1: 811,228-14,750,663	UTS2, RN7SL451P, 376 more genes
nsv3900236	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 5,363,826-18,360,302 , GRCh37 chr1: 5,423,886-18,686,796 , NCBI36 chr1: 5,323,746-18,559,383	UTS2, PDPN, 333 more genes
nsv3888433	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-12,699,337 , GRCh38.p12 chr1: 82,154-12,639,316	UTS2, AURKAIP1, 356 more genes
nsv6636785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276	UTS2, GPR157, 313 more genes
nsv4436105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-11,784,118 , GRCh38.p12 chr1: 82,154-11,724,061	UTS2, PARK7, 325 more genes
nsv3899046	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 844,347-12,470,133 , GRCh37 chr1: 779,727-12,530,188 , NCBI36 chr1: 769,590-12,452,775	UTS2, PRKCZ-DT, 315 more genes
nsv6637093	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897	UTS2, VWA1, 311 more genes
nsv3905483	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 6,303,641-15,799,093 , NCBI36 chr1: 6,286,288-15,998,175 , GRCh37 chr1: 6,363,701-16,125,588	UTS2, VPS13D, 240 more genes
nsv6315409	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-10,258,804 , GRCh38.p12 chr1: 914,086-10,198,746	UTS2, VAMP3, 245 more genes
nsv4436631	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 554,375-9,779,842 , GRCh38.p12 chr1: 618,995-9,719,784	UTS2, LINC02606, 253 more genes
nsv3913374	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 4,737-8,767,973 , GRCh37.p13 chr1: 14,874-8,845,386 , GRCh38.p12 chr1: 14,874-8,785,327	UTS2, LOC105378593, 252 more genes
nsv3907841	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 837,491-9,616,363 , GRCh38 chr1: 902,111-9,556,305 , NCBI36 chr1: 827,354-9,538,950	UTS2, PRKCZ-AS1, 224 more genes
nsv3890178	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 839,329-9,549,767 , GRCh37 chr1: 849,466-9,627,180 , GRCh38 chr1: 914,086-9,567,122	UTS2, ANKRD65, 224 more genes
nsv3885408	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 4,558,588-13,187,457 , GRCh38.p12 chr1: 4,498,528-13,119,984	UTS2, PRAMEF2, 198 more genes
nsv3909850	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 846,680-9,389,984 , GRCh38 chr1: 911,300-9,329,925 , NCBI36 chr1: 836,543-9,312,571	UTS2, LOC105378590, 221 more genes
nsv3903444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 4,958,499-13,178,528 , NCBI36 chr1: 4,858,359-13,101,115 , GRCh38 chr1: 4,898,439-13,111,056	UTS2, NPPA-AS1, 195 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 48

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Number of Variants: 20

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Supplemental Content

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