acer1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 12

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	ACER1, 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	ACER1, 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	ACER1, LENG8, 2408 more genes
nsv3914351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555	ACER1, SEMA6B, 299 more genes
nsv3924102	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622	ACER1, POLR2E, 283 more genes
nsv3890584	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144	ACER1, PCP2, 250 more genes
nsv3923313	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 4,934,897-6,501,653 , GRCh38 chr19: 4,934,885-6,501,642 , NCBI36 chr19: 4,885,897-6,452,653	ACER1, LOC105372253, 47 more genes
nsv3924480	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr19: 5,401,983-6,486,595 , GRCh37.p13 chr19: 5,450,983-6,535,595 , GRCh38.p12 chr19: 5,450,972-6,535,584	ACER1, TINCR, 42 more genes
nsv3918411	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 5,905,175-6,916,287 , GRCh37 chr19: 5,905,186-6,916,298 , NCBI36 chr19: 5,856,186-6,867,298	ACER1, CAPS, 36 more genes
nsv4676137	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 5,949,772-6,699,729 , GRCh38.p12 chr19: 5,949,761-6,699,718	ACER1, MIR6885, 27 more genes
nsv4729892	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 6,096,399-6,699,729 , GRCh38.p12 chr19: 6,096,388-6,699,718	ACER1, TUBB4A, 24 more genes
nsv4676363	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 6,246,138-6,823,741 , GRCh38.p12 chr19: 6,246,127-6,823,730	ACER1, SLC25A23, 26 more genes

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acer1[All Fields] AND 1[has_clinical] (13)
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freshwater metagenome
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