sh3tc2[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
nsv7097514	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 148,426,859-148,427,552 , GRCh38.p12 chr5: 149,047,296-149,047,989	SH3TC2
nsv4450194	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 148,427,405-148,427,572 , GRCh38 chr5: 149,047,842-149,048,009	SH3TC2
nsv6311754	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 148,420,147-148,420,260 , GRCh38.p12 chr5: 149,040,584-149,040,697	SH3TC2
nsv4683468	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 148,420,157-148,420,250 , GRCh38.p12 chr5: 149,040,594-149,040,687	SH3TC2
nsv5674316	insertion	1	nstd102	human	Pathogenic	GRCh37 chr5: 148,407,738-148,407,738 , GRCh38 chr5: 149,028,175-149,028,175	SH3TC2
nsv5674282	insertion	1	nstd102	human	Pathogenic	GRCh37 chr5: 148,407,737-148,407,737 , GRCh38 chr5: 149,028,174-149,028,174	SH3TC2
nsv6636012	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr5: 149,006,277-149,006,376 , GRCh37 chr5: 148,385,840-148,385,939	SH3TC2
nsv3887081	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 149,062,971-149,063,174 , GRCh37 chr5: 148,442,534-148,442,737	SH3TC2, SH3TC2-DT
nsv5673514	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 148,360,713-148,443,737 , GRCh38.p12 chr5: 148,981,150-149,064,174	SH3TC2, MIR584, 2 more genes
nsv6312093	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 148,384,274-148,442,585 , GRCh38.p12 chr5: 149,004,711-149,063,022	SH3TC2, SH3TC2-DT, 2 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	SH3TC2, MEGF10, 2080 more genes
nsv3884357	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440	SH3TC2, TXNDC15, 962 more genes
nsv3912937	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387	SH3TC2, LINC01023, 783 more genes
nsv3878447	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 141,113,273-149,154,835 , GRCh38.p12 chr5: 141,733,706-149,775,272	SH3TC2, LOC107986458, 111 more genes
nsv6636986	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 147,164,969-149,315,489 , GRCh38.p12 chr5: 147,785,406-149,935,926	SH3TC2, GRPEL2-AS1, 43 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	SH3TC2, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	SH3TC2, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	SH3TC2, SPEF2, 2490 more genes
nsv3874238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337	SH3TC2, PJA2, 1228 more genes
nsv3878636	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,125,085-157,574,910 , GRCh38.p12 chr5: 130,789,392-158,147,902	SH3TC2, LOC100288484, 551 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 29

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Number of Variants: 20

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Supplemental Content

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