sdf2l1[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
nsv4729972	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 21,916,216-21,998,113 , GRCh38.p12 chr22: 21,561,927-21,643,824	SDF2L1, UBE2L3, 2 more genes
nsv4674327	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,475,385-23,764,120 , GRCh38.p12 chr22: 17,992,619-23,421,933	SDF2L1, GP1BB, 308 more genes
nsv3917936	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 18,659,766-22,152,986 , GRCh38 chr22: 18,339,130-23,480,799 , GRCh37 chr22: 20,279,766-23,822,986	SDF2L1, IGLV7-46, 298 more genes
nsv3916402	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 21,081,260-24,593,820 , NCBI36 chr22: 19,411,260-22,923,820 , GRCh38 chr22: 20,726,972-24,197,852	SDF2L1, FAM247A, 221 more genes
nsv3897974	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 21,465,661-24,885,806 , GRCh38.p12 chr22: 21,111,372-24,489,838	SDF2L1, IGLV2-34, 214 more genes
nsv3892419	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 20,749,625-23,972,878 , GRCh38.p12 chr22: 20,395,335-23,630,691	SDF2L1, KRT18P5, 217 more genes
nsv3901484	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 21,465,661-24,653,491 , GRCh38.p12 chr22: 21,111,372-24,257,523	SDF2L1, PCAT14, 208 more genes
nsv3904613	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 20,716,876-23,819,697 , GRCh38.p12 chr22: 20,362,586-23,477,510	SDF2L1, LL22NC03-102D1.18, 212 more genes
nsv3922552	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 21,808,950-24,643,108 , NCBI36 chr22: 20,138,950-22,973,108 , GRCh38 chr22: 21,454,661-24,247,140	SDF2L1, IGLJ5, 190 more genes
nsv3917980	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 20,128,104-22,961,613 , GRCh38 chr22: 21,443,815-24,235,645 , GRCh37 chr22: 21,798,104-24,631,613	SDF2L1, IGLV3-12, 190 more genes
nsv3915483	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 20,141,979-22,946,199 , GRCh37 chr22: 21,811,979-24,616,199 , GRCh38 chr22: 21,457,690-24,220,231	SDF2L1, IGLV1-36, 189 more genes
nsv3918766	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 21,562,911-24,307,688 , NCBI36 chr22: 20,247,200-23,033,656 , GRCh37 chr22: 21,917,200-24,703,656	SDF2L1, BCR, 191 more genes
nsv4457780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 21,465,661-23,810,042 , GRCh38.p12 chr22: 21,111,372-23,467,855	SDF2L1, LINC02556, 173 more genes
nsv3894228	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 21,465,661-23,804,835 , GRCh38.p12 chr22: 21,111,372-23,462,648	SDF2L1, IGLJ6, 173 more genes
nsv4729862	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 21,798,906-23,805,099 , GRCh38.p12 chr22: 21,444,617-23,462,912	SDF2L1, LL22NC03-63E9.3, 158 more genes
nsv3909980	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr22: 21,454,661-23,414,686 , GRCh37 chr22: 21,808,950-23,756,873 , NCBI36 chr22: 20,138,950-22,086,873	SDF2L1, LOC102724638, 155 more genes
nsv3923194	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 21,443,815-23,397,298 , NCBI36 chr22: 20,128,104-22,069,485 , GRCh37 chr22: 21,798,104-23,739,485	SDF2L1, IGLV9-49, 156 more genes
nsv4457657	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 21,798,906-23,666,232 , GRCh38.p12 chr22: 21,444,617-23,324,045	SDF2L1, RNA5SP493, 152 more genes
nsv3900410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 21,798,907-23,666,232 , GRCh38.p12 chr22: 21,444,618-23,324,045	SDF2L1, ASH2LP3, 152 more genes
nsv3920622	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 21,454,661-23,312,035 , NCBI36 chr22: 20,138,950-21,984,222 , GRCh37 chr22: 21,808,950-23,654,222	SDF2L1, RIMBP3C, 150 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 101

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Number of Variants: 20

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Supplemental Content

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