stx16[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
nsv7137056	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 58,665,428-58,669,794 , GRCh37 chr20: 57,240,484-57,244,850	STX16, STX16-NPEPL1
nsv4716424	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 58,668,511-58,671,488 , GRCh37 chr20: 57,243,567-57,246,544	STX16, STX16-NPEPL1
nsv7096261	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 57,244,327-57,246,373 , GRCh38.p12 chr20: 58,669,271-58,671,317	STX16, STX16-NPEPL1
nsv4358949	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 57,244,540-57,246,216 , GRCh38.p12 chr20: 58,669,484-58,671,160	STX16, STX16-NPEPL1
nsv6314094	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 55,292,205-57,866,365 , GRCh38.p12 chr20: 56,717,149-59,291,310	STX16, PCK1, 58 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	STX16, 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	STX16, 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	STX16, 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	STX16, 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	STX16, MIR3646, 1310 more genes
nsv3915005	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321	STX16, FTLP1, 472 more genes
nsv6112778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273	STX16, LINC01742, 253 more genes
nsv3911673	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 54,773,088-62,908,674 , NCBI36 chr20: 54,206,495-62,379,118 , GRCh38 chr20: 56,198,032-64,277,321	STX16, LOC105372709, 226 more genes
nsv4357849	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528	STX16, RBM38, 192 more genes
nsv3910216	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 55,804,471-62,904,442 , NCBI36 chr20: 55,237,878-62,374,886 , GRCh38 chr20: 57,229,415-64,273,089	STX16, GID8, 204 more genes
nsv4676332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636	STX16, BMP7, 153 more genes
nsv6314208	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 56,835,739-62,915,555 , GRCh38.p12 chr20: 58,260,683-64,284,202	STX16, LOC105372698, 176 more genes
nsv4676181	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 56,788,101-62,762,405 , GRCh38.p12 chr20: 58,213,045-64,131,052	STX16, LOC105372697, 174 more genes
nsv3894116	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 51,542,616-62,915,555 , GRCh38.p12 chr20: 52,926,077-64,284,202	STX16, ATP5F1E, 254 more genes
nsv3910223	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr20: 51,286,111-62,385,999 , GRCh37 chr20: 51,852,704-62,915,555 , GRCh38 chr20: 53,236,165-64,284,202	STX16, ATP5F1E, 253 more genes

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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 25

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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