OSC1507 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
nsv6629147	copy number variation	10	nstd224	human		GRCh37 chr4: 168,808,600-168,987,754 , GRCh38.p12 chr4: 167,887,449-168,066,603	LOC105377523
nsv6632327	copy number variation	204	nstd224	human		GRCh37 chr8: 137,688,230-137,852,251 , GRCh38.p12 chr8: 136,675,987-136,840,008	LINC02055
nsv6631842	copy number variation	101	nstd224	human		GRCh37 chr7: 142,829,211-142,881,461 , GRCh38.p12 chr7: 143,132,118-143,184,368	PIP, TAS2R39
nsv6624965	copy number variation	22	nstd224	human		GRCh37 chr19: 41,356,319-41,386,033 , GRCh38.p12 chr19: 40,850,414-40,880,128	CYP2A7, CYP2A6
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
nsv6624104	copy number variation	16	nstd224	human		GRCh37 chr17: 61,949,917-61,977,248 , GRCh38.p12 chr17: 63,872,557-63,899,888	CSH1, GH2, 1 more genes
nsv6620485	copy number variation	471	nstd224	human		GRCh37 chr10: 47,543,322-47,703,946 , GRCh38.p12 chr10: 46,172,086-46,332,710	AHCYP1, ANTXRL, 2 more genes
nsv6620190	copy number variation	5	nstd224	human		GRCh37 chr10: 135,256,762-135,373,659 , GRCh38.p12 chr10: 133,443,258-133,560,155	SYCE1, SCART1, 3 more genes
nsv6630221	copy number variation	102	nstd224	human		GRCh37 chr5: 113,160,490-113,171,928 , GRCh38.p12 chr5: 113,824,793-113,836,231	0
nsv6630769	copy number variation	4	nstd224	human		GRCh37 chr6: 168,343,838-168,593,956 , GRCh38.p12 chr6: 167,943,158-168,193,276	KIF25, AFDN, 5 more genes

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