fam83e[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7095721	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 49,118,629-49,120,101 , GRCh38.p12 chr19: 48,615,372-48,616,844	FAM83E, RPL18
nsv3893929	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 49,014,091-49,114,383 , GRCh38.p12 chr19: 48,510,834-48,611,126	FAM83E, SULT2B1, 2 more genes
nsv3893802	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 49,027,683-49,114,383 , GRCh38.p12 chr19: 48,524,426-48,611,126	FAM83E, SPACA4, 1 more genes
nsv3894665	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 49,030,319-49,114,045 , GRCh38.p12 chr19: 48,527,062-48,610,788	FAM83E, SULT2B1, 1 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	FAM83E, 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	FAM83E, 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	FAM83E, LENG8, 2408 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	FAM83E, ZNF461, 735 more genes
nsv3919076	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,432,832-59,083,573 , NCBI36 chr19: 53,124,644-63,775,385 , GRCh38 chr19: 47,929,575-58,572,206	FAM83E, KCNA7, 697 more genes
nsv3911950	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,411,797-59,051,332 , NCBI36 chr19: 53,103,609-63,743,144 , GRCh38 chr19: 47,908,540-58,539,965	FAM83E, LOC107987270, 694 more genes
nsv4676357	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308	FAM83E, MIR4324, 485 more genes
nsv4729755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886	FAM83E, SIGLEC5, 574 more genes
nsv3918983	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 46,658,791-49,050,450 , GRCh37 chr19: 47,162,048-49,553,707 , NCBI36 chr19: 51,853,888-54,245,519	FAM83E, LOC105372432, 121 more genes
nsv4730038	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 48,854,319-49,430,535 , GRCh38.p12 chr19: 48,351,062-48,927,278	FAM83E, BCAT2, 32 more genes
nsv4685764	copy number variation	1	nstd102	human	not provided	GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460	FAM83E, SNAR-G1, 453 more genes
nsv4457853	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 48,119,589-49,595,956 , GRCh38.p12 chr19: 47,616,332-49,092,699	FAM83E, DHDH, 94 more genes
nsv3924184	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 49,080,908-49,342,299 , GRCh38 chr19: 48,577,651-48,839,042 , NCBI36 chr19: 53,772,720-54,034,111	FAM83E, RNU6-317P, 20 more genes

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