fip1l1[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6636923	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 54,228,585-54,361,640 , GRCh38.p12 chr4: 53,362,418-53,495,473	FIP1L1, LOC105377654, 2 more genes
nsv6636708	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 54,169,393-54,283,313 , GRCh38.p12 chr4: 53,303,226-53,417,146	FIP1L1, SCFD2, 1 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	FIP1L1, FTLP10, 335 more genes
nsv3912235	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 52,639,018-59,984,479 , GRCh37 chr4: 53,505,185-60,850,197 , NCBI36 chr4: 53,199,942-60,532,792	FIP1L1, LOC105377672, 97 more genes
nsv6291206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,685,685-58,104,722 , GRCh38.p12 chr4: 51,819,519-57,238,556	FIP1L1, SRD5A3, 96 more genes
nsv3913938	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,736,191-55,968,559 , GRCh38 chr4: 51,870,025-55,102,392 , NCBI36 chr4: 52,430,948-55,663,316	FIP1L1, LINC02260, 42 more genes
nsv6315421	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 53,688,710-56,491,447 , GRCh38.p12 chr4: 52,822,543-55,625,280	FIP1L1, METTL5P3, 38 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	FIP1L1, 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	FIP1L1, 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	FIP1L1, 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	FIP1L1, 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	FIP1L1, 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	FIP1L1, SNHG27, 1091 more genes
nsv3872797	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-66,440,622 , GRCh38.p12 chr4: 68,453-65,574,904	FIP1L1, GNPDA2, 813 more genes
nsv7148157	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396	FIP1L1, OR7E84P, 764 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	FIP1L1, LOC105377297, 582 more genes
nsv3914335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 44,358,218-63,111,600 , NCBI36 chr4: 44,052,975-62,794,195 , GRCh38 chr4: 44,356,201-62,245,882	FIP1L1, RPL22P13, 178 more genes
nsv3910089	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 52,392,545-67,539,802 , GRCh37 chr4: 52,697,788-67,857,207 , GRCh38 chr4: 51,831,622-66,991,489	FIP1L1, LINC02260, 154 more genes
nsv3919213	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,766,026-60,850,197 , NCBI36 chr4: 52,460,783-60,532,792 , GRCh38 chr4: 51,899,860-59,984,479	FIP1L1, LNX1-AS1, 106 more genes
nsv3877501	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 54,027,934-54,386,267 , GRCh38.p12 chr4: 53,161,767-53,520,100	FIP1L1, SCFD2, 4 more genes

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

Send to:

Search results

Items: 1 to 20 of 22

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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 22

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity