npffr2[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
nsv3874679	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 73,000,885-73,003,828 , GRCh38.p12 chr4: 72,135,168-72,138,111	NPFFR2
nsv4674566	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 72,834,889-73,561,412 , GRCh38.p12 chr4: 71,969,172-72,695,695	NPFFR2, ADAMTS3
nsv3915924	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 73,160,675-73,549,259 , GRCh37.p13 chr4: 72,941,811-73,330,395 , GRCh38.p12 chr4: 72,076,094-72,464,678	NPFFR2, ADAMTS3
nsv6291252	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 72,998,352-73,320,894 , GRCh38.p12 chr4: 72,132,635-72,455,177	NPFFR2, ADAMTS3
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	NPFFR2, 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	NPFFR2, 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	NPFFR2, 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	NPFFR2, MICOS10P4, 274 more genes
nsv4674589	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 72,680,879-86,426,232 , GRCh38.p12 chr4: 71,815,162-85,505,079	NPFFR2, SOWAHB, 211 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	NPFFR2, 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	NPFFR2, 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	NPFFR2, 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	NPFFR2, LOC105377262, 126 more genes
nsv4456138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,561,780-78,304,341 , GRCh38.p12 chr4: 70,696,063-77,383,187	NPFFR2, ANKRD17-DT, 119 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	NPFFR2, 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	NPFFR2, 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	NPFFR2, 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	NPFFR2, 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	NPFFR2, 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	NPFFR2, SNHG27, 1091 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 32

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Number of Variants: 20

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Supplemental Content

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