g0s2[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
nsv3881313	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 204,682,513-212,815,646 , GRCh38.p12 chr1: 204,713,385-212,642,304	G0S2, IL19, 184 more genes
nsv3917200	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 206,303,429-210,147,777 , GRCh37.p13 chr1: 208,236,806-212,081,154 , GRCh38.p12 chr1: 208,063,461-211,907,812	G0S2, LOC105372904, 68 more genes
nsv3901751	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 207,756,872-210,332,526 , GRCh38 chr1: 207,583,527-210,159,181 , NCBI36 chr1: 205,823,495-208,399,149	G0S2, LOC105372899, 49 more genes
nsv3870695	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 209,742,722-210,774,573 , GRCh38.p12 chr1: 209,569,377-210,601,229	G0S2, RNASEH1P3, 19 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	G0S2, 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	G0S2, 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	G0S2, RNU1-153P, 4887 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	G0S2, RGS18, 1186 more genes
nsv3881012	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 195,483,439-249,213,000 , GRCh38.p12 chr1: 195,514,309-248,918,801	G0S2, LOC105372928, 1062 more genes
nsv6634372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485	G0S2, LOC105373279, 1036 more genes
nsv4674140	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 204,045,948-249,218,992 , GRCh38.p12 chr1: 204,076,820-248,924,793	G0S2, RNA5S8, 893 more genes
nsv3897747	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 207,346,642-248,930,485 , GRCh37 chr1: 207,519,987-249,224,684 , NCBI36 chr1: 205,586,610-247,191,307	G0S2, RPS18P3, 793 more genes
nsv3890682	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 209,819,552-249,225,312 , NCBI36 chr1: 207,886,175-247,191,935 , GRCh38 chr1: 209,646,207-248,931,113	G0S2, HLX, 749 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	G0S2, 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	G0S2, 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	G0S2, PRELP, 527 more genes
nsv3879807	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 197,811,907-228,997,888 , GRCh38.p12 chr1: 197,842,777-228,862,141	G0S2, RABIF, 637 more genes
nsv3892738	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 204,734,042-225,596,400 , NCBI36 chr1: 203,000,665-223,663,023 , GRCh38 chr1: 204,764,914-225,408,698	G0S2, HLX, 354 more genes
nsv6638068	copy number variation	1	nstd102	human	association	GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753	G0S2, AURKAP1, 372 more genes
nsv5381285	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699	G0S2, DCST1, 2428 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 23

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Number of Variants: 20

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Supplemental Content

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Search details

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