ambn[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
nsv3874321	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,465,502-71,467,849 , GRCh38 chr4: 70,599,785-70,602,132	AMBN
nsv3923759	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502	AMBN, EREG, 530 more genes
nsv5674237	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872	AMBN, FTLP10, 335 more genes
nsv4729598	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,412,409-87,920,784 , GRCh38.p12 chr4: 70,546,692-86,999,632	AMBN, PTPN11P5, 244 more genes
nsv6314916	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 67,833,055-82,716,065 , GRCh37.p13 chr4: 68,698,773-83,637,218	AMBN, MICOS10P4, 274 more genes
nsv3885882	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 58,332,294-71,587,615 , GRCh38.p12 chr4: 57,466,128-70,721,898	AMBN, UBA6-DT, 157 more genes
nsv6313740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 61,867,555-74,711,517 , GRCh38.p12 chr4: 61,001,837-73,845,800	AMBN, CXCL8, 175 more genes
nsv4674141	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,950,363-79,738,598 , GRCh38.p12 chr4: 68,084,645-78,817,444	AMBN, COX18, 216 more genes
nsv3884502	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 66,017,575-76,772,947 , GRCh38.p12 chr4: 65,151,857-75,851,794	AMBN, RNU2-40P, 188 more genes
nsv3913248	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 66,002,875-73,398,274 , GRCh38 chr4: 65,454,562-72,313,693 , GRCh37 chr4: 66,320,280-73,179,410	AMBN, LOC105377262, 126 more genes
nsv3912121	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 67,390,721-71,916,138 , GRCh38 chr4: 66,842,408-70,831,557 , GRCh37 chr4: 67,708,126-71,697,274	AMBN, SPOPLP1, 103 more genes
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	AMBN, LOC100422029, 2358 more genes
nsv3876533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611	AMBN, LOC100420289, 2347 more genes
nsv3884499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286	AMBN, MTND4LP29, 2341 more genes
nsv3880085	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318	AMBN, LOC112268460, 2345 more genes
nsv3883791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495	AMBN, LOC105377343, 2341 more genes
nsv6291432	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354	AMBN, SNHG27, 1091 more genes
nsv3913811	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 51,831,622-97,505,618 , GRCh37 chr4: 52,697,788-98,426,769 , NCBI36 chr4: 52,392,545-98,645,792	AMBN, LOC105377297, 582 more genes
nsv3916323	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 69,551,806-96,215,607 , GRCh38 chr4: 68,686,088-95,294,456 , NCBI36 chr4: 69,234,401-96,434,630	AMBN, UGT2B28, 377 more genes
nsv4456913	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,242,784-82,991,431 , GRCh38.p12 chr4: 67,377,066-82,070,278	AMBN, KPNA2P1, 270 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 27

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Number of Variants: 20

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Supplemental Content

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