heatr1[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3886989	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 236,593,920-236,784,571 , GRCh38.p12 chr1: 236,430,620-236,621,271	HEATR1, ENO1P1, 3 more genes
nsv3871426	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 236,632,983-236,781,478 , GRCh38.p12 chr1: 236,469,683-236,618,178	HEATR1, ENO1P1, 3 more genes
nsv4453396	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr1: 236,604,023-236,787,822 , GRCh38.p12 chr1: 236,440,723-236,624,522	HEATR1, ENO1P1, 3 more genes
nsv4451739	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 236,604,023-236,786,473 , GRCh38.p12 chr1: 236,440,723-236,623,173	HEATR1, LGALS8, 3 more genes
nsv4454086	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 236,604,023-236,778,133 , GRCh38.p12 chr1: 236,440,723-236,614,833	HEATR1, EDARADD, 3 more genes
nsv4453856	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 236,604,210-236,778,133 , GRCh38.p12 chr1: 236,440,910-236,614,833	HEATR1, ENO1P1, 3 more genes
nsv6634337	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 233,012,994-249,206,918 , GRCh38.p12 chr1: 232,877,248-248,912,719	HEATR1, OR2M4, 316 more genes
nsv3904200	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 230,106,271-243,677,283 , NCBI36 chr1: 228,308,641-241,907,208 , GRCh37 chr1: 230,242,018-243,840,585	HEATR1, MIR3123, 221 more genes
nsv7148175	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437	HEATR1, AGT, 221 more genes
nsv3876145	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 235,797,384-249,224,684 , GRCh38.p12 chr1: 235,634,084-248,930,485	HEATR1, OR11L1, 257 more genes
nsv3893126	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 236,719,382-249,212,668 , GRCh38 chr1: 236,556,082-248,918,469 , NCBI36 chr1: 234,786,005-247,179,291	HEATR1, RNU6-1205P, 239 more genes
nsv7148158	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 235,215,476-247,005,888 , GRCh37.p13 chr1: 235,378,791-247,169,190	HEATR1, RNU6-747P, 172 more genes
nsv6636217	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 232,732,121-243,338,216 , GRCh38.p12 chr1: 232,596,375-243,174,914	HEATR1, LINC01347, 169 more genes
nsv3912845	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 230,713,047-240,722,962 , GRCh37.p13 chr1: 232,646,424-242,656,339 , GRCh38.p12 chr1: 232,510,678-242,493,037	HEATR1, RNU4-77P, 158 more genes
nsv3881799	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 232,226,609-241,010,904 , GRCh38.p12 chr1: 232,090,863-240,847,604	HEATR1, MIPEPP2, 137 more genes
nsv3870910	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 236,617,216-244,515,378 , GRCh38.p12 chr1: 236,453,916-244,352,076	HEATR1, RNU6-725P, 103 more genes
nsv3889025	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 234,605,553-240,932,205 , GRCh38.p12 chr1: 234,469,807-240,768,905	HEATR1, MIR4428, 102 more genes
nsv6112661	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 231,407,943-237,289,859 , GRCh38.p12 chr1: 231,272,197-237,126,559	HEATR1, LOC105373207, 113 more genes
nsv4346874	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 234,742,890-239,475,761 , GRCh38.p12 chr1: 234,607,144-239,312,461	HEATR1, LINC01348, 82 more genes
nsv4674008	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 233,843,930-237,971,511 , GRCh38.p12 chr1: 233,708,184-237,808,211	HEATR1, LGALS8-AS1, 75 more genes

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

Send to:

Search results

Items: 1 to 20 of 63

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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 63

Page of 4

Number of Variants: 20

Page of 4

Supplemental Content

Find related data

Search details

Recent activity