rhog[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
nsv6634327	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927	RHOG, SNORA54, 219 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	RHOG, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	RHOG, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	RHOG, IGHMBP2, 2829 more genes
nsv3898926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-37,698,540 , GRCh38.p12 chr11: 230,615-37,676,990	RHOG, OR51L1, 771 more genes
nsv4674879	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449	RHOG, BGLT3, 723 more genes
nsv3906221	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673	RHOG, PCNAP4, 688 more genes
nsv6315535	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599	RHOG, OR52Q1P, 630 more genes
nsv3894525	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-25,584,362 , GRCh38.p12 chr11: 230,615-25,562,816	RHOG, SDHCP4, 620 more genes
nsv3912558	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 446,754-18,926,289 , GRCh38 chr11: 446,754-18,904,742 , NCBI36 chr11: 436,754-18,882,865	RHOG, TRIM22, 546 more genes
nsv3898948	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-17,099,213 , GRCh38.p12 chr11: 230,615-17,077,666	RHOG, MTND5P21, 506 more genes
nsv4350476	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589	RHOG, KRTAP5-3, 457 more genes
nsv3919565	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092	RHOG, OR51A7, 437 more genes
nsv3892294	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-9,704,511 , GRCh38.p12 chr11: 230,615-9,682,964	RHOG, MRPS24P1, 405 more genes
nsv4768373	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811	RHOG, LOC107984302, 375 more genes
nsv6637864	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177	RHOG, PNPLA2, 372 more genes
nsv3918376	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 128,203-5,440,733 , GRCh37.p13 chr11: 138,203-5,484,157 , GRCh38.p12 chr11: 138,203-5,462,927	RHOG, HBG2, 262 more genes
nsv3913735	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 196,855-5,343,104 , GRCh38 chr11: 196,855-5,321,874 , NCBI36 chr11: 186,855-5,299,680	RHOG, CDKN1C, 246 more genes
nsv3894576	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 193,187-5,291,338 , GRCh38.p12 chr11: 193,187-5,270,108	RHOG, SSU72L4, 243 more genes
nsv4729112	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307	RHOG, OR51E1, 203 more genes

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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 30

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Number of Variants: 20

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Supplemental Content

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