scfd2[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
nsv3878178	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 53,961,609-54,067,101 , GRCh38.p12 chr4: 53,095,442-53,200,934	SCFD2
nsv4455616	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 53,926,759-54,031,101 , GRCh38.p12 chr4: 53,060,592-53,164,934	SCFD2
nsv4674204	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 54,139,333-54,203,666 , GRCh38.p12 chr4: 53,273,166-53,337,499	SCFD2
nsv3921012	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 53,736,956-53,876,597 , GRCh37.p13 chr4: 54,042,199-54,181,840 , GRCh38.p12 chr4: 53,176,032-53,315,673	SCFD2, RNU6-310P
nsv6636355	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 53,715,514-53,925,549 , GRCh38.p12 chr4: 52,849,347-53,059,382	SCFD2, RASL11B, 1 more genes
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	SCFD2, 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	SCFD2, LOC105377654, 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	SCFD2, 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	SCFD2, 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	SCFD2, 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	SCFD2, 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	SCFD2, 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	SCFD2, 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	SCFD2, 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	SCFD2, 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	SCFD2, 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	SCFD2, 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	SCFD2, 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	SCFD2, 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	SCFD2, OR7E84P, 764 more genes

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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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