rap1gap2[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
nsv3906895	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr17: 2,901,448-2,940,028 , GRCh38.p12 chr17: 2,998,154-3,036,734	RAP1GAP2
nsv3923263	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr17: 2,692,218-2,952,376 , GRCh37 chr17: 2,745,468-3,005,626 , GRCh38 chr17: 2,842,174-3,102,332	RAP1GAP2, LOC101927911, 2 more genes
nsv3913013	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055	RAP1GAP2, RPS4XP17, 289 more genes
nsv3915884	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 45,835-6,862,369 , GRCh38 chr17: 162,088-6,959,050 , NCBI36 chr17: 11,879-6,803,093	RAP1GAP2, LOC105371592, 222 more genes
nsv3922546	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 525-5,779,421 , GRCh38 chr17: 150,732-5,935,377 , GRCh37 chr17: 525-5,838,697	RAP1GAP2, CHRNE, 198 more genes
nsv4674912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088	RAP1GAP2, SRR, 196 more genes
nsv3913795	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 43,098-5,496,266 , GRCh37 chr17: 45,835-5,555,542 , GRCh38 chr17: 193,307-5,652,222	RAP1GAP2, BHLHA9, 194 more genes
nsv3921779	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 87,039-4,585,577 , GRCh38 chr17: 237,248-4,735,533 , GRCh37 chr17: 396,627-4,638,828	RAP1GAP2, ARRB2, 146 more genes
nsv3919819	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 50,690-4,168,935 , NCBI36 chr17: 48,539-4,115,684 , GRCh38 chr17: 198,748-4,265,640	RAP1GAP2, LOC105371430, 125 more genes
nsv3904699	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-3,871,323 , GRCh38.p12 chr17: 157,423-3,968,029	RAP1GAP2, OVCA2, 120 more genes
nsv3892866	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-3,825,428 , GRCh38.p12 chr17: 150,732-3,922,134	RAP1GAP2, OR1P1, 120 more genes
nsv3920266	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 226,472-3,655,099 , NCBI36 chr17: 76,263-3,505,142 , GRCh37 chr17: 396,627-3,558,393	RAP1GAP2, RN7SL624P, 107 more genes
nsv3902288	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 48,858-3,379,400 , GRCh38.p12 chr17: 199,067-3,476,106	RAP1GAP2, GEMIN4, 100 more genes
nsv3920795	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 2,062,380-5,258,340 , NCBI36 chr17: 1,912,424-5,102,359 , GRCh37 chr17: 1,965,674-5,161,635	RAP1GAP2, LINC01996, 128 more genes
nsv3913766	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 150,732-3,242,868 , NCBI36 chr17: 525-3,092,912 , GRCh37 chr17: 525-3,146,162	RAP1GAP2, LOC105371483, 90 more genes
nsv3919726	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 50,690-3,005,626 , NCBI36 chr17: 48,539-2,952,376 , GRCh38 chr17: 198,748-3,102,332	RAP1GAP2, RN7SL608P, 81 more genes
nsv3906989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 48,858-2,940,028 , GRCh38.p12 chr17: 199,067-3,036,734	RAP1GAP2, GEMIN4, 79 more genes
nsv3902798	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-2,750,745 , GRCh38.p12 chr17: 150,732-2,847,451	RAP1GAP2, WDR81, 80 more genes
nsv3892504	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 2,050,166-4,315,506 , GRCh38.p12 chr17: 2,146,872-4,412,211	RAP1GAP2, OR3A2, 73 more genes
nsv6112772	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 2,313,096-3,735,525 , GRCh38.p12 chr17: 2,409,802-3,832,231	RAP1GAP2, LOC105371592, 49 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 69

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Number of Variants: 20

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