sgcb[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
nsv4450427	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 52,023,947-52,038,269 , GRCh37 chr4: 52,890,113-52,904,435	SGCB
nsv6311727	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr4: 52,890,123-52,904,425 , GRCh38.p12 chr4: 52,023,957-52,038,259	SGCB
nsv7096856	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,894,124-52,896,039 , GRCh38.p12 chr4: 52,027,958-52,029,873	SGCB
nsv7097255	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,899,577-52,899,826 , GRCh38.p12 chr4: 52,033,411-52,033,660	SGCB
nsv4682626	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr4: 52,899,587-52,899,816 , GRCh38.p12 chr4: 52,033,421-52,033,650	SGCB
nsv3873898	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 52,038,207-52,038,279 , GRCh37 chr4: 52,904,373-52,904,445	SGCB
nsv7093525	insertion	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,894,225-52,894,225 , GRCh38 chr4: 52,028,059-52,028,059	SGCB
nsv7096734	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 52,890,123-52,890,346 , GRCh38.p12 chr4: 52,023,957-52,024,180	SGCB
nsv3872830	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr4: 52,023,937-52,038,279 , GRCh37 chr4: 52,890,103-52,904,445	SGCB
nsv3889721	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 52,899,577-52,899,826 , GRCh38 chr4: 52,033,411-52,033,660	SGCB
nsv3887995	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 52,903,470-52,927,077 , GRCh38.p12 chr4: 52,037,304-52,060,911	SGCB, SPATA18, 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	SGCB, FTLP10, 335 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	SGCB, 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	SGCB, LINC02260, 42 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	SGCB, 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	SGCB, 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	SGCB, 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	SGCB, 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	SGCB, 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	SGCB, 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

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Items: 1 to 20 of 29

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Number of Variants: 20

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