OSC4480 AND nstd224 - dbVar - NCBI

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6626541	copy number variation	6	nstd224	human		GRCh37 chr20: 14,803,454-14,827,620 , GRCh38.p12 chr20: 14,822,808-14,846,974	MACROD2
nsv6628116	copy number variation	277	nstd224	human		GRCh37 chr2: 38,956,836-38,972,328 , GRCh38.p12 chr2: 38,729,694-38,745,186	SRSF7, GALM
nsv6624232	copy number variation	259	nstd224	human		GRCh37 chr17: 34,450,463-34,461,869 , GRCh38.p12 chr17: 36,123,077-36,134,487 , GRCh38.p12 chr17\|NT_187661.1: 77,174-88,584 , GRCh38.p12 chr17\|NT_187614.1: 357,991-369,397	LOC101927369, LOC107985055
nsv6623053	copy number variation	3	nstd224	human		GRCh37 chr15: 24,530,736-24,728,780 , GRCh38.p12 chr15: 24,285,589-24,483,633	PWRN3, LOC102725165, 2 more genes
nsv6624930	copy number variation	25	nstd224	human		GRCh37 chr19: 43,262,353-43,344,686 , GRCh38.p12 chr19: 42,758,201-42,840,534	CEACAMP6, PSG8-AS1, 2 more genes
nsv6627726	copy number variation	214	nstd224	human		GRCh37 chr2: 179,300,979-179,315,726 , GRCh38.p12 chr2: 178,436,252-178,450,999	PRKRA, PJVK, 1 more genes
nsv6628233	copy number variation	60	nstd224	human		GRCh37 chr2: 89,442,329-90,229,318 , GRCh38.p12 chr2: 89,142,846-90,190,466	IGKV6D-21, IGKV3D-25, 59 more genes
nsv6630105	copy number variation	12	nstd224	human		GRCh37 chr5: 140,214,995-140,228,262 , GRCh38.p12 chr5: 140,835,410-140,848,677	PCDHA7, PCDHA4, 8 more genes
nsv6632848	copy number variation	1	nstd224	human		GRCh37 chr8: 89,514,775-90,681,455 , GRCh38.p12 chr8: 88,502,546-89,669,227	KRT8P4, LOC105375629, 4 more genes
nsv6628545	copy number variation	1	nstd224	human		GRCh37 chr3: 178,960,744-179,207,592 , GRCh38.p12 chr3: 179,242,956-179,489,804	KCNMB3, ZNF639, 5 more genes

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