steap1[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
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	STEAP1, 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	STEAP1, LOC107986817, 2014 more genes
nsv3914094	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 84,002,634-95,228,883 , GRCh37 chr7: 83,631,950-94,858,195 , NCBI36 chr7: 83,469,886-94,696,131	STEAP1, LINC03017, 121 more genes
nsv3915862	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 88,152,747-89,637,882 , GRCh37 chr7: 88,314,811-89,799,946 , GRCh38 chr7: 88,685,497-90,170,632	STEAP1, TEX47, 7 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	STEAP1, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	STEAP1, RPL23AP51, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	STEAP1, MNX1-AS2, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	STEAP1, TRGV3, 2682 more genes
nsv6313801	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 77,821,356-93,340,137 , GRCh38.p12 chr7: 78,192,039-93,710,825	STEAP1, SOCS5P1, 140 more genes
nsv5381780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704	STEAP1, ARPC1A, 265 more genes
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	STEAP1, AOC1, 2682 more genes
nsv4352523	inversion	1	nstd102	human	Pathogenic	GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550	STEAP1, ACHE, 1532 more genes
nsv3915824	copy number variation	2	nstd102	human	Uncertain significance, Conflicting interpretations of pathogenicity	GRCh37 chr7: 88,192,865-89,799,946 , NCBI36 chr7: 88,030,801-89,637,882 , GRCh38 chr7: 88,563,550-90,170,632	STEAP1, TEX47, 10 more genes
nsv3917092	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr7: 86,846,728-91,199,124 , GRCh37 chr7: 87,008,792-91,361,188 , GRCh38 chr7: 87,379,476-91,731,873	STEAP1, CDK14, 44 more genes
nsv3920135	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr7: 88,030,801-89,950,219 , GRCh37.p13 chr7: 88,192,865-90,112,283 , GRCh38.p12 chr7: 88,563,550-90,482,969	STEAP1, LOC107986816, 20 more genes
nsv3907740	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 88,146,318-89,895,850 , GRCh38.p12 chr7: 88,517,003-90,266,536	STEAP1, CFAP69, 13 more genes
nsv3922464	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 88,149,358-89,890,810 , GRCh38 chr7: 88,520,043-90,261,496 , NCBI36 chr7: 87,987,294-89,728,746	STEAP1, STEAP2-AS1, 13 more genes
nsv3901236	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 88,146,318-89,884,701 , GRCh38.p12 chr7: 88,517,003-90,255,387	STEAP1, ZNF804B, 13 more genes
nsv3897476	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 88,337,283-89,884,701 , GRCh38.p12 chr7: 88,707,969-90,255,387	STEAP1, LOC107986817, 10 more genes
nsv3919680	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 88,353,926-89,882,647 , GRCh38 chr7: 88,724,612-90,253,333 , NCBI36 chr7: 88,191,862-89,720,583	STEAP1, DPY19L2P4, 10 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 44

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Number of Variants: 20

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