smpx[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
nsv7098613	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 21,755,681-21,772,408 , GRCh38.p12 chrX: 21,737,563-21,754,290	SMPX
nsv6290497	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 21,606,718-21,780,720 , GRCh38.p12 chrX: 21,588,600-21,762,602	SMPX, KLHL34, 1 more genes
nsv6635997	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 21,606,719-21,774,071 , GRCh38.p12 chrX: 21,588,601-21,755,953	SMPX, KLHL34, 1 more genes
nsv6312981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 21,606,718-21,773,954 , GRCh38.p12 chrX: 21,588,600-21,755,836	SMPX, CNKSR2, 1 more genes
nsv4674802	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 21,261,124-21,835,952 , GRCh38.p12 chrX: 21,243,006-21,817,834	SMPX, KLHL34, 3 more genes
nsv3875749	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 21,406,789-21,764,818 , GRCh38.p12 chrX: 21,388,671-21,746,700	SMPX, CNKSR2, 2 more genes
nsv6313047	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 21,755,681-22,266,301 , GRCh38.p12 chrX: 21,737,563-22,248,184	SMPX, PHEX, 6 more genes
nsv3904162	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754	SMPX, NANOGNBP3, 2154 more genes
nsv3913255	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895	SMPX, NHS-AS1, 2154 more genes
nsv3907094	copy number variation	4	nstd102	human	Pathogenic	GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065	SMPX, GPR119, 2153 more genes
nsv3878553	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100	SMPX, H2AB2, 2152 more genes
nsv3898149	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 20,297-156,026,127 , NCBI36 chrX: 10,297-154,908,986 , GRCh37 chrX: 70,297-155,255,792	SMPX, OR3B1P, 2154 more genes
nsv3877395	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174	SMPX, ARMCX2, 2154 more genes
nsv3884935	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127	SMPX, NDUFB11, 2154 more genes
nsv3903061	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chrX: 679-154,896,026 , GRCh38 chrX: 10,679-156,013,167 , GRCh37 chrX: 60,679-155,242,832	SMPX, SLC38A5, 2152 more genes
nsv3885865	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 70,297-155,246,585 , GRCh38.p12 chrX: 20,297-156,016,920	SMPX, MIR1277, 2152 more genes
nsv6112690	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301	SMPX, LOC105373176, 2151 more genes
nsv3907545	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 64,245-155,228,958 , NCBI36 chrX: 4,245-154,882,152 , GRCh38 chrX: 14,245-155,999,293	SMPX, TMEM30BP1, 2151 more genes
nsv3884029	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 71,267-155,224,766 , GRCh38.p12 chrX: 21,267-155,995,101	SMPX, SSX4B, 2150 more genes
nsv3898185	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 76,102-155,226,096 , NCBI36 chrX: 16,102-154,879,290 , GRCh38 chrX: 26,102-155,996,431	SMPX, ANKRD11P2, 2151 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 161

Page of 9

Number of Variants: 20

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