srsf12[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
nsv3880626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 85,988,428-120,548,687 , GRCh38.p12 chr6: 85,278,710-120,227,541	SRSF12, LOC107986534, 426 more genes
nsv3921478	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 76,692,636-93,477,232 , GRCh38 chr6: 75,926,199-92,710,793 , GRCh37 chr6: 76,635,916-93,420,511	SRSF12, SPACA1, 187 more genes
nsv3923528	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 84,604,741-99,376,910 , GRCh38 chr6: 83,838,303-98,822,313 , GRCh37 chr6: 84,548,022-99,270,189	SRSF12, RNU4-72P, 157 more genes
nsv3914309	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 82,569,098-93,753,476 , NCBI36 chr6: 83,335,534-94,519,915 , GRCh37 chr6: 83,278,815-94,463,194	SRSF12, ME1, 136 more genes
nsv3873582	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 83,319,012-91,907,669 , GRCh38.p12 chr6: 82,609,295-91,197,951	SRSF12, LOC105377882, 117 more genes
nsv3918084	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 86,513,991-93,898,976 , GRCh38 chr6: 85,804,273-93,189,258 , NCBI36 chr6: 86,570,710-93,955,697	SRSF12, LOC105377897, 91 more genes
nsv3912992	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 85,370,716-90,669,793 , NCBI36 chr6: 86,137,153-91,436,233 , GRCh37 chr6: 86,080,434-91,379,512	SRSF12, DNAJC19P6, 88 more genes
nsv4675039	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 86,024,761-90,023,713 , GRCh38.p12 chr6: 85,315,043-89,313,994	SRSF12, C6orf163, 65 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	SRSF12, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	SRSF12, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	SRSF12, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	SRSF12, ITPR3, 2905 more genes
nsv3919111	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637	SRSF12, RNU6-770P, 810 more genes
nsv6313857	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492	SRSF12, LOC101928570, 288 more genes
nsv3872975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 81,261,418-97,796,269 , GRCh38.p12 chr6: 80,551,701-97,348,393	SRSF12, ME1, 178 more genes
nsv6634392	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297	SRSF12, MTHFD2P2, 212 more genes
nsv4456405	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 87,627,836-93,698,486 , GRCh38.p12 chr6: 86,918,118-92,988,768	SRSF12, MIR4643, 82 more genes
nsv4455227	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 88,783,642-96,282,103 , GRCh38.p12 chr6: 88,073,924-95,834,227	SRSF12, MDN1, 65 more genes
nsv3922502	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 89,774,237-90,472,036 , GRCh37 chr6: 89,717,518-90,415,315 , GRCh38 chr6: 89,007,799-89,705,596	SRSF12, RN7SL11P, 17 more genes
nsv3885958	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 89,720,586-90,415,315 , GRCh38.p12 chr6: 89,010,867-89,705,596	SRSF12, PM20D2, 17 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 21

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Number of Variants: 20

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Supplemental Content

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Search details

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