ros1[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
nsv4728879	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 117,683,820-117,766,264 , GRCh38.p12 chr6: 117,362,657-117,445,101	ROS1, RAP1BP3
nsv3884321	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 117,493,311-117,728,118 , GRCh38.p12 chr6: 117,172,148-117,406,955	ROS1, LOC105377964, 3 more genes
nsv3889901	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 117,572,602-117,619,588 , GRCh38.p12 chr6: 117,251,439-117,298,425	ROS1, LOC105377964, 2 more genes
nsv3880626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 85,988,428-120,548,687 , GRCh38.p12 chr6: 85,278,710-120,227,541	ROS1, LOC107986534, 426 more genes
nsv6313858	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488	ROS1, RN7SL509P, 311 more genes
nsv3924576	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 97,164,591-122,524,393 , GRCh38 chr6: 96,609,994-122,161,548 , GRCh37 chr6: 97,057,870-122,482,694	ROS1, TUBE1, 318 more genes
nsv3920683	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 109,372,795-132,430,553 , GRCh37 chr6: 109,266,102-132,388,860 , GRCh38 chr6: 108,944,899-132,067,720	ROS1, SSXP10, 298 more genes
nsv3910417	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 100,054,889-120,488,154 , NCBI36 chr6: 100,609,486-120,850,999 , GRCh37 chr6: 100,502,765-120,809,300	ROS1, LINC02518, 266 more genes
nsv3924741	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 106,951,594-126,102,365 , GRCh38 chr6: 106,503,719-125,781,219 , NCBI36 chr6: 107,058,287-126,144,058	ROS1, LOC105377979, 266 more genes
nsv6315321	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 115,941,808-133,892,653 , GRCh37.p13 chr6: 116,262,971-134,213,791	ROS1, SLC18B1, 223 more genes
nsv7148249	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 113,857,248-130,442,177 , GRCh37.p13 chr6: 114,178,427-130,763,322	ROS1, TRDN-AS1, 179 more genes
nsv3924661	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 115,601,230-128,514,324 , GRCh37 chr6: 115,922,394-128,835,469 , NCBI36 chr6: 116,029,087-128,877,162	ROS1, MCM9, 146 more genes
nsv4457007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 110,981,075-119,608,396 , GRCh38.p12 chr6: 110,659,872-119,287,231	ROS1, HDAC2-AS2, 134 more genes
nsv3918326	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 116,145,074-123,993,898 , GRCh37.p13 chr6: 116,038,381-123,952,199 , GRCh38.p12 chr6: 115,717,217-123,631,054	ROS1, MCM9, 93 more genes
nsv4768325	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 116,734,559-123,648,104 , GRCh38.p12 chr6: 116,413,396-123,326,959	ROS1, GJA1, 80 more genes
nsv1398251	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 112,511,751-118,037,596 , GRCh38.p12 chr6: 112,190,549-117,716,433	ROS1, RPSAP45, 82 more genes
nsv3881153	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 113,261,042-117,842,826 , GRCh38.p12 chr6: 112,939,840-117,521,663	ROS1, NT5DC1, 63 more genes
nsv1398200	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 116,681,080-119,775,014 , GRCh38.p12 chr6: 116,359,917-119,453,849	ROS1, GPRC6A, 48 more genes
nsv7097176	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 116,441,236-119,252,888 , GRCh38.p12 chr6: 116,120,073-118,931,723	ROS1, RN7SKP18, 49 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	ROS1, LOC105378061, 2914 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 34

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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