"estd216"[study] AND "duplication"[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
esv3648116	copy number variation	1	estd216	human	not provided	GRCh38.p12 chr2: 153,845,295-154,275,106 , GRCh37 chr2: 154,701,808-155,131,619	GALNT13
esv3648670	copy number variation	1	estd216	human	not provided	GRCh38.p12 chr2: 135,214,523-135,473,889 , GRCh37 chr2: 135,972,093-136,231,459	ZRANB3
esv3648187	copy number variation	1	estd216	human	not provided	GRCh38.p12 chr4: 85,289,128-85,511,228 , GRCh37 chr4: 86,210,281-86,432,381	ARHGAP24
esv3648773	copy number variation	1	estd216	human	not provided	GRCh38.p12 chr15: 81,685,124-81,795,773 , GRCh37 chr15: 81,977,465-82,088,114	LOC105370921
esv3648854	copy number variation	1	estd216	human	not provided	GRCh37 chr18: 30,901,989-31,009,751 , GRCh38.p12 chr18: 33,322,025-33,429,787	CCDC178
esv3648380	copy number variation	1	estd216	human	not provided	GRCh37 chr7: 111,069,946-111,166,165 , GRCh38.p12 chr7: 111,429,890-111,526,109	IMMP2L
esv3648147	copy number variation	1	estd216	human	not provided	GRCh37 chr3: 163,178,778-163,263,886 , GRCh38.p12 chr3: 163,460,990-163,546,098	RNU7-82P
esv3648935	copy number variation	1	estd216	human	not provided	GRCh37 chr20: 12,807,016-12,889,314 , GRCh38.p12 chr20: 12,826,368-12,908,666	LINC01722
esv3648626	copy number variation	1	estd216	human	not provided	GRCh37 chr3: 35,826,707-35,902,885 , GRCh38.p12 chr3: 35,785,215-35,861,393	ARPP21
esv3648692	copy number variation	1	estd216	human	not provided	GRCh38.p12 chr13: 89,764,094-89,838,629 , GRCh37 chr13: 90,387,429-90,490,883	RPL7L1P1
esv3648155	copy number variation	1	estd216	human	not provided	GRCh37 chr3: 173,239,453-173,309,839 , GRCh38.p12 chr3: 173,521,663-173,592,049	NLGN1
esv3648722	copy number variation	1	estd216	human	not provided	GRCh38.p12 chr2: 39,291,371-39,361,656 , GRCh37 chr2: 39,518,512-39,588,797	MAP4K3
esv3648324	copy number variation	1	estd216	human	not provided	GRCh38.p12 chr6: 124,083,394-124,153,450 , GRCh37 chr6: 124,404,539-124,474,595	NKAIN2
esv3648208	copy number variation	1	estd216	human	not provided	GRCh38.p12 chr4: 161,024,150-161,088,373 , GRCh37 chr4: 161,945,302-162,009,525	LOC105377514
esv3648154	copy number variation	1	estd216	human	not provided	GRCh37 chr3: 173,239,453-173,301,037 , GRCh38.p12 chr3: 173,521,663-173,583,247	NLGN1
esv3648650	copy number variation	1	estd216	human	not provided	GRCh38.p12 chr12: 124,776,099-124,836,915 , GRCh37 chr12: 125,260,645-125,321,461	SCARB1
esv3648559	copy number variation	1	estd216	human	not provided	GRCh38.p12 chr2: 123,060,720-123,121,016 , GRCh37 chr2: 123,818,296-123,878,592	LINC01826
esv3648325	copy number variation	1	estd216	human	not provided	GRCh38.p12 chr6: 124,095,702-124,153,450 , GRCh37 chr6: 124,416,847-124,474,595	NKAIN2
esv3648209	copy number variation	1	estd216	human	not provided	GRCh38.p12 chr4: 161,031,076-161,088,373 , GRCh37 chr4: 161,952,228-162,009,525	LOC105377514
esv3648330	copy number variation	1	estd216	human	not provided	GRCh38.p12 chr6: 147,348,950-147,402,441 , GRCh37 chr6: 147,670,086-147,723,577	STXBP5

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Number of Variants: 20

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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 249

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Number of Variants: 20

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