upk3b[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
nsv3899795	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 76,123,879-76,144,695 , GRCh38.p12 chr7: 76,494,562-76,515,378 , GRCh38.p12 chr7\|NT_187561.1: 1-14,465	UPK3B, DTX2
nsv3896004	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 76,132,879-76,144,695 , GRCh38.p12 chr7: 76,503,562-76,515,378 , GRCh38.p12 chr7\|NT_187561.1: 2,581-14,465	UPK3B, DTX2
nsv3876629	copy number variation	1	nstd102	human	not provided	GRCh38 chr7: 76,504,886-76,515,243 , GRCh37 chr7: 76,134,203-76,144,560	UPK3B, DTX2
esv3648367	copy number variation	1	estd216	human	not provided	GRCh37 chr7: 76,134,203-76,144,560 , GRCh38.p12 chr7: 76,504,886-76,515,243 , GRCh38.p12 chr7\|NT_187561.1: 3,905-14,330	UPK3B, DTX2
nsv3916696	copy number variation	2	nstd102	human	Benign	GRCh37 chr7: 76,139,282-76,558,024 , GRCh38 chr7: 76,509,965-76,928,707 , NCBI36 chr7: 75,977,218-76,395,960	UPK3B, SPDYE16, 3 more genes
nsv3911011	copy number variation	1	nstd102	human	Benign/Likely benign	NCBI36 chr7: 75,977,222-76,395,008 , GRCh37 chr7: 76,139,286-76,557,072 , GRCh38 chr7: 76,509,969-76,927,755	UPK3B, LOC105375358, 3 more genes
nsv3921452	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 76,139,286-76,511,841 , GRCh38 chr7: 76,509,969-76,882,524 , NCBI36 chr7: 75,977,222-76,349,777	UPK3B, POMZP3, 2 more genes
nsv3894902	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 76,069,874-76,144,695 , GRCh38.p12 chr7: 76,440,557-76,515,378	UPK3B, DTX2, 2 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	UPK3B, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	UPK3B, LOC107986817, 2014 more genes
nsv3918722	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 71,225,344-81,735,657 , GRCh37 chr7: 70,690,330-81,364,973 , NCBI36 chr7: 70,328,266-81,202,909	UPK3B, GTF2IP1, 184 more genes
nsv3922762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 73,992,744-83,618,176 , GRCh38 chr7: 73,873,420-83,988,860 , NCBI36 chr7: 72,925,686-83,456,112	UPK3B, PMS2P3, 142 more genes
nsv3911276	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 69,382,353-77,823,832 , GRCh37 chr7: 68,847,339-77,453,149 , NCBI36 chr7: 68,485,275-77,291,085	UPK3B, POM121, 155 more genes
nsv3917211	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 74,377,395-82,031,742 , NCBI36 chr7: 73,429,661-81,498,994 , GRCh37 chr7: 73,992,744-81,661,058	UPK3B, HSPB1, 123 more genes
nsv3902523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 75,588,704-80,277,632 , GRCh38.p12 chr7: 75,959,386-80,648,316	UPK3B, GSAP, 72 more genes
nsv4728820	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,403,117-76,709,600 , GRCh38.p12 chr7: 72,932,579-77,080,283	UPK3B, FDPSP7, 119 more genes
nsv6290688	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 75,058,300-79,083,658 , GRCh37.p13 chr7: 75,921,853-78,712,974	UPK3B, GTF2IP1, 76 more genes
nsv3922160	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 72,404,249-76,189,514 , GRCh38 chr7: 73,352,304-76,722,261 , GRCh37 chr7: 72,766,313-76,351,578	UPK3B, PMS2P10, 88 more genes
nsv3921264	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 74,963,960-77,842,828 , GRCh37 chr7: 75,126,024-78,004,892 , GRCh38 chr7: 75,496,701-78,375,575	UPK3B, PMS2P11, 56 more genes
nsv3912641	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 74,904,287-76,093,741 , GRCh37.p13 chr7\|NW_003871064.1: 2,966,309-3,821,770 , GRCh37.p13 chr7: 75,066,351-76,255,805 , GRCh38.p12 chr7: 75,437,073-76,626,488	UPK3B, YWHAG, 29 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 63

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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