spock3[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
nsv6291173	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 168,034,701-168,115,705 , GRCh38.p12 chr4: 167,113,550-167,194,554	SPOCK3
nsv4674594	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 167,490,481-167,693,089 , GRCh38.p12 chr4: 166,569,329-166,771,938	SPOCK3
nsv6636633	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 167,428,990-167,860,888 , GRCh38.p12 chr4: 166,507,838-166,939,737	SPOCK3, RNA5SP171
nsv3920660	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 168,324,472-168,729,033 , GRCh37.p13 chr4: 168,087,897-168,492,458 , GRCh38.p12 chr4: 167,166,746-167,571,307	SPOCK3, RN7SL776P
nsv6634395	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 166,940,253-167,778,165 , GRCh38.p12 chr4: 166,019,101-166,857,014	SPOCK3, TLL1, 1 more genes
nsv3888872	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr4: 167,634,638-168,841,223 , GRCh38.p12 chr4: 166,713,487-167,920,072	SPOCK3, RN7SKP188, 3 more genes
nsv4674532	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 166,967,503-167,656,201 , GRCh38.p12 chr4: 166,046,351-166,735,050	SPOCK3, RNA5SP170, 1 more genes
nsv6634351	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318	SPOCK3, COPS3P1, 363 more genes
nsv4674043	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 165,010,461-190,957,473 , GRCh38.p12 chr4: 164,089,309-190,036,318	SPOCK3, CYP4V2, 319 more genes
nsv3912039	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 164,039,530-189,982,708 , GRCh37 chr4: 164,960,682-190,828,225 , NCBI36 chr4: 165,180,132-191,140,857	SPOCK3, CYP4V2, 314 more genes
nsv3916579	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 166,202,188-190,939,340 , GRCh38 chr4: 165,281,036-190,018,185 , NCBI36 chr4: 166,421,638-191,176,334	SPOCK3, LOC105377614, 291 more genes
nsv4456171	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 166,623,890-190,957,473 , GRCh38.p12 chr4: 165,702,738-190,036,318	SPOCK3, TRIML2, 284 more genes
nsv3913994	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 166,317,587-190,095,391 , GRCh37 chr4: 167,238,739-190,828,225 , NCBI36 chr4: 167,458,189-191,250,527	SPOCK3, PTGES3P3, 290 more genes
nsv6634364	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318	SPOCK3, LOC101928551, 279 more genes
nsv3886420	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 162,205,710-182,329,883 , GRCh38.p12 chr4: 161,284,558-181,408,730	SPOCK3, RPL35AP12, 187 more genes
nsv3919458	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 155,162,982-170,959,553 , GRCh37 chr4: 156,084,134-171,880,704 , NCBI36 chr4: 156,303,584-172,117,279	SPOCK3, AIDAP2, 172 more genes
nsv3878182	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 162,344,510-177,103,037 , GRCh38.p12 chr4: 161,423,358-176,181,886	SPOCK3, LINC02504, 156 more genes
nsv5381776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 157,771,352-172,496,278 , GRCh38.p12 chr4: 156,850,200-171,575,127	SPOCK3, LOC107986326, 144 more genes
nsv3917143	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 167,551,358-180,742,113 , GRCh38 chr4: 166,630,207-179,820,960 , NCBI36 chr4: 167,770,808-180,979,107	SPOCK3, HPF1, 122 more genes
nsv3918711	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 162,723,818-172,501,433 , GRCh37 chr4: 163,644,970-173,422,584 , NCBI36 chr4: 163,864,420-173,659,159	SPOCK3, LOC101928081, 104 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 58

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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