bmper[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
nsv4675847	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 33,868,997-34,247,759 , GRCh38.p12 chr7: 33,829,385-34,208,147	BMPER
nsv6312860	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 34,125,348-34,192,885 , GRCh38.p12 chr7: 34,085,736-34,153,273	BMPER
nsv6313625	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 34,089,097-34,113,817 , GRCh38.p12 chr7: 34,049,485-34,074,205	BMPER
nsv4455187	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 33,914,258-34,015,196 , GRCh38.p12 chr7: 33,874,646-33,975,584	BMPER
nsv3914287	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr7: 33,739,493-34,439,143 , GRCh37 chr7: 33,772,968-34,472,618 , GRCh38 chr7: 33,733,356-34,433,006	BMPER, RNU6-438P, 1 more genes
nsv3912299	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr7: 33,603,723-34,360,889 , GRCh37.p13 chr7: 33,637,198-34,394,364 , GRCh38.p12 chr7: 33,597,586-34,354,752	BMPER, FLJ20712, 3 more genes
nsv4684247	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 33,643,418-34,089,823 , GRCh38.p12 chr7: 33,603,806-34,050,211	BMPER, BBS9, 1 more genes
nsv4675636	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 33,667,313-34,047,534 , GRCh38.p12 chr7: 33,627,701-34,007,922	BMPER, BBS9, 1 more genes
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	BMPER, 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	BMPER, LOC107986817, 2014 more genes
nsv3897424	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 32,911,003-44,576,005 , GRCh38.p12 chr7: 32,871,391-44,536,406	BMPER, LOC107986734, 192 more genes
nsv3912277	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 32,684,528-41,051,106 , GRCh37 chr7: 32,718,003-41,084,581 , GRCh38 chr7: 32,678,391-41,044,983	BMPER, MATCAP2, 134 more genes
nsv6636445	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 27,133,786-34,466,477 , GRCh38.p12 chr7: 27,094,167-34,426,865	BMPER, MIR550A1, 119 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	BMPER, 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	BMPER, 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	BMPER, 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	BMPER, TRGV3, 2682 more genes
nsv3915802	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-41,915,483 , GRCh38 chr7: 54,185-41,875,885 , NCBI36 chr7: 149,268-41,882,008	BMPER, RPL23AP52, 638 more genes
nsv3899194	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 11,048,840-52,863,626 , GRCh38.p12 chr7: 11,009,213-52,795,933	BMPER, BRWD1P3, 590 more genes
nsv3918785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-37,129,317 , NCBI36 chr7: 149,268-37,095,842 , GRCh38 chr7: 54,185-37,089,712	BMPER, MMD2, 554 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 31

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Number of Variants: 20

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Supplemental Content

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