"estd216"[study] AND "deletion"[variant_type] - 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
esv3648710	copy number variation	1	estd216	human	not provided	GRCh37 chr2: 35,819,686-36,085,059 , GRCh38.p12 chr2: 35,594,620-35,859,993	MRPL50P1
esv3648462	copy number variation	1	estd216	human	not provided	GRCh37 chr8: 137,679,805-137,857,327 , GRCh38.p12 chr8: 136,667,562-136,845,084	LINC02055
esv3648463	copy number variation	1	estd216	human	not provided	GRCh37 chr8: 137,688,230-137,857,327 , GRCh38.p12 chr8: 136,675,987-136,845,084	LINC02055
esv3648188	copy number variation	1	estd216	human	not provided	GRCh37 chr4: 93,786,775-93,948,103 , GRCh38.p12 chr4: 92,865,624-93,026,952	GRID2
esv3648343	copy number variation	1	estd216	human	not provided	GRCh37 chr7: 10,819,155-10,945,193 , GRCh38.p12 chr7: 10,779,528-10,905,566	MGC4859
esv3648846	copy number variation	1	estd216	human	not provided	GRCh37 chr18: 1,725,758-1,841,469 , GRCh38.p12 chr18: 1,725,757-1,841,468 , GRCh38.p12 chr18\|NW_019805503.1: 1-119,817	LOC105371959
esv3648469	copy number variation	1	estd216	human	not provided	GRCh37 chr9: 3,628,376-3,747,376 , GRCh38.p12 chr9: 3,628,376-3,747,376	RFX3-DT
esv3648474	copy number variation	1	estd216	human	not provided	GRCh37 chr9: 12,046,842-12,163,583 , GRCh38.p12 chr9: 12,046,842-12,163,583	LOC105375976
esv3648847	copy number variation	1	estd216	human	not provided	GRCh37 chr18: 1,725,758-1,839,339 , GRCh38.p12 chr18: 1,725,757-1,839,338 , GRCh38.p12 chr18\|NW_019805503.1: 1-95,134	LOC105371959
esv3648189	copy number variation	1	estd216	human	not provided	GRCh37 chr4: 97,308,914-97,391,366 , GRCh38.p12 chr4: 96,387,763-96,470,215	LINC02267
esv3648309	copy number variation	1	estd216	human	not provided	GRCh37 chr6: 65,828,853-65,910,220 , GRCh38.p12 chr6: 65,118,960-65,200,327	EYS
esv3648429	copy number variation	1	estd216	human	not provided	GRCh37 chr8: 15,948,235-16,025,964 , GRCh38.p12 chr8: 16,090,726-16,168,455	MSR1
esv3648428	copy number variation	1	estd216	human	not provided	GRCh37 chr8: 15,948,235-16,025,964 , GRCh38.p12 chr8: 16,090,726-16,168,455	MSR1
esv3648132	copy number variation	1	estd216	human	not provided	GRCh37 chr1: 73,011,443-73,086,201 , GRCh38.p12 chr1: 72,545,760-72,620,518	LOC105378797
esv3648602	copy number variation	1	estd216	human	not provided	GRCh37 chr11: 120,557,343-120,630,452 , GRCh38.p12 chr11: 120,686,634-120,759,743	GRIK4
esv3648601	copy number variation	1	estd216	human	not provided	GRCh37 chr11: 120,557,343-120,630,452 , GRCh38.p12 chr11: 120,686,634-120,759,743	GRIK4
esv3648186	copy number variation	1	estd216	human	not provided	GRCh37 chr4: 80,871,932-80,943,688 , GRCh38.p12 chr4: 79,950,778-80,022,534	ANTXR2
esv3648453	copy number variation	1	estd216	human	not provided	GRCh37 chr8: 86,923,375-86,990,451 , GRCh38.p12 chr8: 85,911,146-85,978,222	LOC107986954
esv3648760	copy number variation	1	estd216	human	not provided	GRCh37 chr2: 51,345,474-51,411,126 , GRCh38.p12 chr2: 51,118,336-51,183,988	NRXN1-DT
esv3648603	copy number variation	1	estd216	human	not provided	GRCh37 chr11: 122,686,128-122,749,214 , GRCh38.p12 chr11: 122,815,420-122,878,506	CRTAM

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dbVar

Result Filters

Object Type

Organism

Variant Type

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Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Study Type

Subject Phenotype Status

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Items: 1 to 20 of 630

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Number of Variants: 20

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