ubb[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
nsv3919368	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 15,704,477-20,556,000 , GRCh37.p13 chr17: 15,763,752-20,615,408 , GRCh38.p12 chr17: 15,860,438-20,712,095	UBB, CCDC144A, 196 more genes
nsv3910522	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 15,754,173-20,552,548 , GRCh38 chr17: 15,850,859-20,649,235 , NCBI36 chr17: 15,694,898-20,493,140	UBB, EEF1A1P43, 196 more genes
nsv3917007	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 15,573,932-20,354,156 , GRCh37 chr17: 15,633,207-20,413,564 , GRCh38 chr17: 15,729,893-20,510,251	UBB, LRRC75A, 193 more genes
nsv3922067	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 15,727,076-20,501,923 , GRCh38 chr17: 15,883,037-20,658,018 , GRCh37 chr17: 15,786,351-20,561,331	UBB, KRT16P4, 196 more genes
nsv3922810	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 15,883,037-20,620,700 , GRCh37 chr17: 15,786,351-20,524,013 , NCBI36 chr17: 15,727,076-20,464,605	UBB, SNORD49B, 194 more genes
nsv3923405	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 15,742,071-20,464,605 , GRCh38 chr17: 15,898,032-20,620,700 , GRCh37 chr17: 15,801,346-20,524,013	UBB, RPL21P121, 194 more genes
nsv3908020	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 15,745,315-20,261,191 , GRCh38.p12 chr17: 15,842,001-20,357,878	UBB, PEMT, 173 more genes
nsv4675003	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 15,632,431-18,726,389 , GRCh38.p12 chr17: 15,729,117-18,823,076	UBB, LLGL1, 127 more genes
nsv3918054	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 15,776,915-18,771,753 , NCBI36 chr17: 15,620,954-18,615,791 , GRCh37 chr17: 15,680,229-18,675,066	UBB, TBC1D27P, 121 more genes
nsv4729738	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 15,810,015-18,537,436 , GRCh38.p12 chr17: 15,906,701-18,634,123	UBB, UPF3AP1, 109 more genes
nsv3923105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 15,855,385-18,266,133 , NCBI36 chr17: 15,796,110-18,206,858 , GRCh38 chr17: 15,952,071-18,362,819	UBB, NEK4P2, 89 more genes
nsv3913316	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 14,910,841-17,316,496 , GRCh38 chr17: 15,066,799-17,472,457 , GRCh37 chr17: 14,970,116-17,375,771	UBB, CDRT3, 86 more genes
nsv3913412	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 16,021,199-18,266,133 , GRCh38 chr17: 16,117,885-18,362,819 , NCBI36 chr17: 15,961,924-18,206,858	UBB, EEF1A1P43, 83 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	UBB, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	UBB, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	UBB, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	UBB, SMURF2, 2366 more genes
nsv3917939	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 10,892,259-17,964,282 , NCBI36 chr17: 10,736,301-17,808,321 , GRCh37 chr17: 10,795,576-17,867,596	UBB, MIR744, 139 more genes
nsv6315277	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 11,915,997-17,892,664 , GRCh37.p13 chr17: 11,819,314-17,795,978	UBB, LINC02087, 135 more genes
nsv3921507	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 15,259,164-20,925,299 , GRCh37 chr17: 15,162,481-20,828,612 , NCBI36 chr17: 15,103,206-20,769,204	UBB, SCDP1, 232 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 42

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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