rgs21[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
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	RGS21, CRB1, 1608 more genes
nsv3874431	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 171,990,029-195,086,758 , GRCh38.p12 chr1: 172,020,889-195,117,628	RGS21, PTGS2, 307 more genes
nsv3888143	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 179,413,479-201,764,737 , GRCh38.p12 chr1: 179,444,344-201,795,609	RGS21, CSRP1-AS1, 273 more genes
nsv4673925	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 177,551,193-199,599,056 , GRCh38.p12 chr1: 177,582,058-199,629,928	RGS21, QSOX1, 263 more genes
nsv3878624	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 179,073,386-200,192,265 , GRCh38.p12 chr1: 179,104,251-200,223,137	RGS21, LOC105371661, 249 more genes
nsv3905741	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 179,002,040-199,694,025 , NCBI36 chr1: 177,268,663-197,960,648 , GRCh38 chr1: 179,032,905-199,724,897	RGS21, SLC4A1APP2, 240 more genes
nsv3877653	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 179,011,314-199,022,759 , GRCh38.p12 chr1: 179,042,179-199,053,630	RGS21, LINC02818, 234 more genes
nsv3896481	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 176,595,962-196,301,688 , GRCh37 chr1: 176,565,098-196,270,818 , NCBI36 chr1: 174,831,721-194,537,441	RGS21, RN7SL230P, 231 more genes
nsv3897058	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 189,003,614-199,584,994 , NCBI36 chr1: 187,270,237-197,851,617 , GRCh38 chr1: 189,034,483-199,615,866	RGS21, LINC02770, 89 more genes
nsv3872374	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 191,919,194-194,615,758 , GRCh37 chr1: 191,888,324-194,584,888	RGS21, MIR4426, 31 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	RGS21, MARK1, 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	RGS21, SNAP47, 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	RGS21, RNU1-153P, 4887 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	RGS21, LOC101060227, 1608 more genes
nsv4450583	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041	RGS21, RGS18, 1186 more genes
nsv3895767	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 187,143,981-224,299,417 , NCBI36 chr1: 185,379,736-222,553,742 , GRCh37 chr1: 187,113,113-224,487,119	RGS21, LOC107985458, 590 more genes
nsv3889347	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 185,644,663-221,698,833 , GRCh38.p12 chr1: 185,675,531-221,525,491	RGS21, MIR1231, 543 more genes
nsv6636965	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906	RGS21, PRELP, 527 more genes
nsv6636659	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr1: 189,633,885-199,854,163 , GRCh38.p12 chr1: 189,664,755-199,885,035	RGS21, F13B, 88 more genes
nsv4674607	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 191,542,979-192,297,254 , GRCh38.p12 chr1: 191,573,849-192,328,124	RGS21, LOC647150, 4 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 22

Page of 2

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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