brd9[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
nsv3924048	copy number variation	1	nstd102	human	Benign	NCBI36 chr5: 763,494-943,017 , GRCh37 chr5: 710,494-890,017 , GRCh38 chr5: 710,379-889,902	BRD9, ZDHHC11, 2 more genes
nsv4457065	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 855,268-975,647 , GRCh38.p12 chr5: 855,153-975,532	BRD9, TRIP13, 1 more genes
nsv3914649	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 22,149-35,831,538 , GRCh37 chr5: 22,149-35,831,640 , NCBI36 chr5: 75,149-35,867,397	BRD9, LOC105374666, 399 more genes
nsv3887142	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-34,041,196 , GRCh38.p12 chr5: 22,149-34,041,091	BRD9, H3Y1, 381 more genes
nsv3910712	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 166,576-34,034,151 , GRCh38 chr5: 113,461-33,998,289 , GRCh37 chr5: 113,576-33,998,394	BRD9, ROPN1L, 378 more genes
nsv3924496	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-32,248,116 , NCBI36 chr5: 75,149-32,283,873 , GRCh38 chr5: 22,149-32,248,010	BRD9, LOC105374678, 356 more genes
nsv6636942	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932	BRD9, LOC105374608, 351 more genes
nsv6636606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420	BRD9, BASP1, 338 more genes
nsv3881706	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-31,343,671 , GRCh38.p12 chr5: 25,329-31,343,564	BRD9, IRX2-DT, 339 more genes
nsv3883796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-30,672,798 , GRCh38.p12 chr5: 25,329-30,672,691	BRD9, H3P22, 335 more genes
nsv6315416	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-30,712,376 , GRCh38.p12 chr5: 113,461-30,712,269	BRD9, LOC105374649, 333 more genes
nsv3912696	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 50,093-30,112,642 , GRCh38 chr5: 49,978-30,112,535 , NCBI36 chr5: 103,093-30,148,399	BRD9, OTULINL, 333 more genes
nsv5381771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716	BRD9, OTULINL, 317 more genes
nsv3916877	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-28,625,056 , GRCh37 chr5: 22,149-28,589,299 , GRCh38 chr5: 22,149-28,589,192	BRD9, CTD-2154B17.1, 313 more genes
nsv3922865	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 22,149-28,429,241 , GRCh37 chr5: 22,149-28,429,348 , NCBI36 chr5: 75,149-28,465,105	BRD9, CCT6P2, 312 more genes
nsv3916127	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-27,824,480 , GRCh37 chr5: 22,149-27,788,723 , GRCh38 chr5: 22,149-27,788,616	BRD9, LOC101929898, 310 more genes
nsv3914997	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-27,611,270 , GRCh38 chr5: 22,149-27,611,163 , NCBI36 chr5: 75,149-27,647,027	BRD9, LINC02241, 309 more genes
nsv3917481	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 22,149-27,485,619 , NCBI36 chr5: 75,149-27,521,483 , GRCh37 chr5: 22,149-27,485,726	BRD9, LOC645763, 309 more genes
nsv3923396	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-27,188,057 , NCBI36 chr5: 75,149-27,223,814 , GRCh38 chr5: 22,149-27,187,950	BRD9, LINC02899, 307 more genes
nsv3887688	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-26,948,599 , GRCh38.p12 chr5: 113,461-26,948,492	BRD9, LINC02223, 304 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 145

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Number of Variants: 20

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Supplemental Content

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Search details

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