OSC2523 AND nstd224 - dbVar - NCBI

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Items: 9

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6624351	copy number variation	1	nstd224	human		GRCh37 chr17: 77,192,453-77,234,671 , GRCh38.p12 chr17: 79,196,371-79,238,589	RBFOX3
nsv6627890	copy number variation	2	nstd224	human		GRCh37 chr2: 53,595,922-53,835,083 , GRCh38.p12 chr2: 53,368,784-53,607,946	LOC105374600, RNU6-997P
nsv6622877	copy number variation	8	nstd224	human		GRCh37 chr15: 30,950,529-31,088,443 , GRCh38.p12 chr15: 30,658,326-30,796,240 , GRCh38.p12 chr15\|NT_187660.1: 2,943,865-3,081,952 , GRCh38.p12 chr15\|NW_011332701.1: 2,831,413-2,969,500	LOC100288637, LOC101930434
nsv6630884	copy number variation	168	nstd224	human		GRCh37 chr5: 814,876-825,329 , GRCh38.p12 chr5: 814,761-825,214	ZDHHC11, SPCS2P3
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
nsv6628875	copy number variation	412	nstd224	human		GRCh37 chr3: 75,453,294-75,554,281 , GRCh38.p12 chr3: 75,404,143-75,505,130	ENPP7P2, LINC02018, 2 more genes
nsv6627055	copy number variation	71	nstd224	human		GRCh37 chr22: 18,892,575-19,008,108 , GRCh38.p12 chr22: 18,905,062-19,020,595	DGCR6, PRODH, 1 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
nsv6630005	copy number variation	1	nstd224	human		GRCh37 chr5: 101,291,960-101,364,700 , GRCh38.p12 chr5: 101,956,256-102,028,996	0

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