septin11[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
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	SEPTIN11, EREG, 530 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	SEPTIN11, 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	SEPTIN11, 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	SEPTIN11, SOWAHB, 211 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	SEPTIN11, COX18, 216 more genes
nsv3922666	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 76,597,345-85,234,472 , GRCh38 chr4: 75,453,111-84,094,295 , GRCh37 chr4: 76,378,321-85,015,448	SEPTIN11, LOC100421142, 146 more genes
nsv6313715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 73,055,313-80,083,154 , GRCh38.p12 chr4: 72,189,596-79,162,000	SEPTIN11, CCNG2, 129 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	SEPTIN11, 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	SEPTIN11, 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	SEPTIN11, 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	SEPTIN11, 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	SEPTIN11, 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	SEPTIN11, 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	SEPTIN11, 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	SEPTIN11, 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	SEPTIN11, UGT2B28, 377 more genes
nsv6313510	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 75,737,340-91,131,156 , GRCh38.p12 chr4: 74,812,130-90,210,005	SEPTIN11, HIGD1AP13, 240 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	SEPTIN11, KPNA2P1, 270 more genes
nsv3920040	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 72,262,258-86,002,147 , GRCh37 chr4: 73,127,975-86,923,300 , NCBI36 chr4: 73,346,839-87,142,324	SEPTIN11, SNORD144, 212 more genes
nsv3922248	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 72,213,455-79,239,266 , GRCh37 chr4: 71,994,591-79,020,242 , GRCh38 chr4: 71,128,874-78,099,088	SEPTIN11, GC, 123 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 24

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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