suz12[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
nsv3917955	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr17: 27,339,633-27,352,368 , GRCh37.p13 chr17: 30,315,520-30,328,255 , GRCh38.p12 chr17: 31,988,501-32,001,236	SUZ12
nsv3899228	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 30,300,563-30,377,162 , GRCh38.p12 chr17: 31,973,544-32,050,143	SUZ12, SH3GL1P1, 1 more genes
nsv3919950	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 24,298,969-27,841,151 , GRCh37 chr17: 27,274,843-30,817,038 , GRCh38 chr17: 28,947,825-32,490,020	SUZ12, MIR365B, 105 more genes
nsv3895059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,578,241-32,142,196 , GRCh38.p12 chr17: 31,251,223-33,815,177	SUZ12, RNU6-1134P, 48 more genes
nsv4729951	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,989,741-32,355,632 , GRCh38.p12 chr17: 31,662,722-34,028,613	SUZ12, RNA5SP437, 34 more genes
nsv3910415	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 25,976,412-27,410,628 , GRCh38 chr17: 30,625,268-32,059,496 , GRCh37 chr17: 28,952,286-30,386,515	SUZ12, GPR160P2, 42 more genes
nsv4349804	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 28,993,036-30,412,788 , GRCh38.p12 chr17: 30,666,018-32,085,769	SUZ12, LOC105371725, 39 more genes
nsv3924565	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 26,017,162-27,436,901 , GRCh38 chr17: 30,666,018-32,085,769 , GRCh37 chr17: 28,993,036-30,412,788	SUZ12, UTP6, 39 more genes
nsv6290215	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 28,992,701-30,408,700 , GRCh38.p12 chr17: 30,665,683-32,081,681	SUZ12, MIR4733, 38 more genes
nsv4457440	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 28,999,903-30,409,337 , GRCh38.p12 chr17: 30,672,885-32,082,318	SUZ12, MIR365B, 38 more genes
nsv3897082	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,003,358-30,412,788 , GRCh38.p12 chr17: 30,676,340-32,085,769	SUZ12, RNU6-298P, 39 more genes
nsv3902844	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 28,959,760-30,367,155 , GRCh38.p12 chr17: 30,632,742-32,040,136	SUZ12, LOC101927057, 41 more genes
nsv3913159	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 26,029,297-27,424,998 , GRCh38 chr17: 30,678,153-32,073,866 , GRCh37 chr17: 29,005,171-30,400,885	SUZ12, RNU6ATAC7P, 38 more genes
nsv3893120	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 28,997,893-30,391,813 , GRCh38.p12 chr17: 30,670,875-32,064,794	SUZ12, RN7SL45P, 38 more genes
nsv3890075	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 28,993,036-30,386,515 , GRCh38.p12 chr17: 30,666,018-32,059,496	SUZ12, RN7SL79P, 38 more genes
nsv3902358	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 28,997,791-30,386,515 , GRCh38.p12 chr17: 30,670,773-32,059,496	SUZ12, LOC646030, 38 more genes
nsv4578269	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 28,941,066-30,326,958 , GRCh38.p12 chr17: 30,614,048-31,999,939	SUZ12, LOC105371723, 41 more genes
nsv4729791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,039,844-30,412,788 , GRCh38.p12 chr17: 30,712,826-32,085,769	SUZ12, ADAP2, 37 more genes
nsv4457704	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,054,315-30,409,336 , GRCh38.p12 chr17: 30,727,297-32,082,317	SUZ12, SH3GL1P1, 36 more genes
nsv3920118	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 26,036,063-27,372,534 , GRCh37 chr17: 29,011,937-30,348,421 , GRCh38 chr17: 30,684,919-32,021,402	SUZ12, MIR193A, 37 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 49

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Number of Variants: 20

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