cd22[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3919296	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723	CD22, UBA2, 241 more genes
nsv3916007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990	CD22, MAG, 238 more genes
nsv3918197	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 31,367,353-35,417,098 , NCBI36 chr19: 36,550,099-40,599,840 , GRCh37 chr19: 31,858,259-35,908,000	CD22, LINC01531, 110 more genes
nsv4349605	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090	CD22, ATP4A, 129 more genes
nsv4350190	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 35,043,556-36,316,644 , GRCh38.p12 chr19: 34,552,651-35,825,742	CD22, SCN1B, 76 more genes
nsv4674329	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 35,553,425-36,264,299 , GRCh38.p12 chr19: 35,062,521-35,773,397	CD22, LOC105372379, 50 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	CD22, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	CD22, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	CD22, LENG8, 2408 more genes
nsv3913730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354	CD22, BCKDHA, 1102 more genes
nsv6290300	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324	CD22, ZNF420, 574 more genes
nsv4457372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575	CD22, ZNF461, 735 more genes
nsv3900139	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 30,735,448-36,120,396 , GRCh38.p12 chr19: 30,244,541-35,629,494	CD22, ZNF599, 130 more genes
nsv3906538	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 35,658,728-36,173,537 , GRCh38.p12 chr19: 35,167,825-35,682,635	CD22, ATP4A, 33 more genes
nsv4676336	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 35,811,335-35,898,248 , GRCh38.p12 chr19: 35,320,432-35,407,346	CD22, EEF1A1P7, 5 more genes
nsv6310629	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 35,521,725-36,643,309 , GRCh38.p12 chr19: 35,030,821-36,152,407	CD22, KRTDAP, 78 more genes
nsv4457800	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 35,613,953-36,183,886 , GRCh38.p12 chr19: 35,123,049-35,692,984	CD22, SBSN, 38 more genes
nsv7095478	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407	CD22, NFKBID, 141 more genes
nsv1398275	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 35,516,999-35,990,896 , GRCh38.p12 chr19: 35,026,095-35,499,994	CD22, LOC105372380, 30 more genes

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