bhlhe23[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
nsv3902122	copy number variation	1	nstd102	human	Benign	GRCh37 chr20: 61,595,624-61,637,326 , GRCh38.p12 chr20: 62,964,272-63,005,974	BHLHE23, SLC17A9
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	BHLHE23, 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	BHLHE23, 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	BHLHE23, 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	BHLHE23, 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	BHLHE23, 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	BHLHE23, 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	BHLHE23, 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	BHLHE23, 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	BHLHE23, 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	BHLHE23, GID8, 60 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	BHLHE23, 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	BHLHE23, 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	BHLHE23, 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	BHLHE23, LINC01749, 32 more genes
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	BHLHE23, TGIF2-RAB5IF, 1314 more genes
nsv3905072	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435	BHLHE23, LRRN4, 1313 more genes
nsv3895314	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202	BHLHE23, PKIG, 1311 more genes
nsv3896520	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110	BHLHE23, COMMD7, 1311 more genes
nsv3920218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118	BHLHE23, MIR3646, 1310 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 57

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Number of Variants: 20

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