map4[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3885257	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 47,980,175-47,986,210 , GRCh38.p12 chr3: 47,938,685-47,944,720	MAP4
nsv3876051	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 47,980,305-48,092,017 , GRCh38.p12 chr3: 47,938,815-48,050,527	MAP4, VPS26BP1
nsv6315166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376	MAP4, TMEM89, 129 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	MAP4, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	MAP4, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	MAP4, RPL23AP49, 2875 more genes
nsv4347762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589	MAP4, UQCRC1, 291 more genes
nsv3921797	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 45,896,379-50,762,357 , GRCh38 chr3: 45,879,883-50,749,922 , GRCh37 chr3: 45,921,375-50,787,353	MAP4, RBM5-AS1, 185 more genes
nsv3883164	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 37,028,313-49,929,220 , GRCh38.p12 chr3: 36,986,822-49,891,787	MAP4, ACAA1, 344 more genes
nsv3875386	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 47,899,878-48,348,163 , GRCh38.p12 chr3: 47,858,388-48,306,673	MAP4, NME6, 13 more genes
nsv4451853	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 47,927,728-48,206,720 , GRCh38.p12 chr3: 47,886,238-48,165,230	MAP4, RPL17P16, 4 more genes
nsv4674044	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 47,970,377-48,227,462 , GRCh38.p12 chr3: 47,928,887-48,185,972	MAP4, RN7SL664P, 6 more genes
nsv7096805	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318	MAP4, SNORA94, 120 more genes
nsv4453258	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 47,799,614-48,359,988 , GRCh38.p12 chr3: 47,758,124-48,318,498	MAP4, MRPS18AP1, 17 more genes
nsv7096956	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 47,422,587-47,919,033 , GRCh38.p12 chr3: 47,381,097-47,877,543	MAP4, BOLA2P2, 12 more genes
nsv3919716	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 47,884,484-48,276,485 , GRCh38 chr3: 47,867,990-48,259,991 , GRCh37 chr3: 47,909,480-48,301,481	MAP4, CDC25A, 10 more genes

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