birc7[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
nsv6314131	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,003,263-62,915,555 , GRCh38.p12 chr20: 62,428,207-64,284,202	BIRC7, HAR1A, 100 more genes
nsv4676208	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,152,321-62,915,555 , GRCh38.p12 chr20: 62,555,114-64,284,202	BIRC7, GMEB2, 94 more genes
nsv3916163	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,211,869-62,908,674 , GRCh38 chr20: 62,561,794-64,277,321 , NCBI36 chr20: 60,569,446-62,379,118	BIRC7, LOC105372727, 94 more genes
nsv3916631	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,179,280-62,915,555 , NCBI36 chr20: 60,589,725-62,385,999 , GRCh38 chr20: 62,582,073-64,284,202	BIRC7, PTK6, 91 more genes
nsv3922590	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 60,553,022-62,343,283 , GRCh38 chr20: 62,545,370-64,241,486 , GRCh37 chr20: 61,142,577-62,872,839	BIRC7, RPL7P3, 95 more genes
nsv3913089	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 60,765,104-62,385,999 , GRCh37 chr20: 61,294,659-62,915,555 , GRCh38 chr20: 62,663,307-64,284,202	BIRC7, SLCO4A1-AS1, 89 more genes
nsv3922908	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 61,010,752-62,435,964 , GRCh37.p13 chr20: 61,540,307-62,965,520 , GRCh38.p12 chr20: 62,908,955-64,334,167	BIRC7, NPBWR2, 78 more genes
nsv3911578	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 62,455,231-63,839,491 , NCBI36 chr20: 60,463,682-61,941,288 , GRCh37 chr20: 61,030,287-62,470,844	BIRC7, LOC105372716, 70 more genes
nsv6314091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,619,222-62,915,555 , GRCh38.p12 chr20: 62,987,870-64,284,202	BIRC7, TPD52L2, 72 more genes
nsv7148178	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 62,632,017-63,794,804 , GRCh37.p13 chr20: 61,267,734-62,426,157	BIRC7, GID8, 60 more genes
nsv6291738	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,775,756-62,915,555 , GRCh38.p12 chr20: 63,144,404-64,284,202	BIRC7, PTK6, 63 more genes
nsv3911666	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,785,315-62,908,674 , GRCh38 chr20: 63,153,963-64,277,321 , NCBI36 chr20: 61,255,760-62,379,118	BIRC7, MIR3196, 63 more genes
nsv3900085	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,827,144-62,907,526 , GRCh38.p12 chr20: 63,195,792-64,276,173	BIRC7, PCMTD2, 62 more genes
nsv3909648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,827,144-62,907,467 , GRCh38.p12 chr20: 63,195,792-64,276,114	BIRC7, LOC100130587, 62 more genes
nsv3903709	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,429,900-62,293,991 , GRCh38.p12 chr20: 62,798,548-63,662,638	BIRC7, RNU6-994P, 48 more genes
nsv3918154	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 60,936,175-61,769,233 , GRCh37.p13 chr20: 61,465,730-62,298,789 , GRCh38.p12 chr20: 62,834,378-63,667,436	BIRC7, COL20A1, 45 more genes
nsv5381809	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,510,452-62,315,381 , GRCh38.p12 chr20: 62,879,100-63,684,028	BIRC7, MIR3196, 40 more genes
nsv7095910	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,471,874-62,078,210 , GRCh38.p12 chr20: 62,840,522-63,446,857	BIRC7, LINC01749, 32 more genes
nsv6314138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,797,521-62,318,983 , GRCh38.p12 chr20: 63,166,169-63,687,630	BIRC7, HELZ2, 27 more genes
nsv6290292	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,828,010-62,324,686 , GRCh38.p12 chr20: 63,196,658-63,693,333	BIRC7, GMEB2, 26 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 67

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Number of Variants: 20

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Supplemental Content

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Search details

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