adap2[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
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	ADAP2, MIR365B, 105 more genes
nsv7095086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 27,573,882-29,576,157 , GRCh38.p12 chr17: 29,246,864-31,249,139	ADAP2, LOC107984990, 59 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	ADAP2, SUZ12, 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	ADAP2, 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	ADAP2, 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	ADAP2, 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	ADAP2, 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	ADAP2, 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	ADAP2, 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	ADAP2, 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	ADAP2, 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	ADAP2, 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	ADAP2, 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	ADAP2, 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	ADAP2, TEFM, 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	ADAP2, 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	ADAP2, MIR193A, 37 more genes
nsv3911512	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 26,023,960-27,351,071 , GRCh37 chr17: 28,999,834-30,326,958 , GRCh38 chr17: 30,672,816-31,999,939	ADAP2, MIR4724, 36 more genes
nsv3923073	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 26,057,989-27,351,065 , GRCh37 chr17: 29,033,863-30,326,952 , GRCh38 chr17: 30,706,845-31,999,933	ADAP2, LOC105371723, 35 more genes
nsv3900910	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 29,033,882-30,326,958 , GRCh38.p12 chr17: 30,706,864-31,999,939	ADAP2, MIR4733HG, 35 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 63

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Number of Variants: 20

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