OSC2878 AND nstd224 - dbVar - NCBI

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Items: 10

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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
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
nsv6625378	copy number variation	31	nstd224	human		GRCh37 chr1: 1,386,089-1,431,163 , GRCh38.p12 chr1: 1,450,709-1,495,783	ATAD3C, ATAD3B
nsv6623223	copy number variation	7	nstd224	human		GRCh37 chr16: 3,705,380-3,716,031 , GRCh38.p12 chr16: 3,655,379-3,666,030	DNASE1, TRAP1
nsv6620185	copy number variation	4	nstd224	human		GRCh37 chr10: 135,015,095-135,032,385 , GRCh38.p12 chr10: 133,201,591-133,218,881	LOC105378573, KNDC1
nsv6626824	copy number variation	7	nstd224	human		GRCh37 chr20: 58,440,438-58,514,677 , GRCh38.p12 chr20: 59,865,383-59,939,622	FAM217B, PPP1R3D, 1 more genes
nsv6630970	copy number variation	19	nstd224	human		GRCh37 chr6: 31,356,574-31,453,618 , GRCh38.p12 chr6: 31,388,797-31,485,841	HCP5, HLA-X, 5 more genes
nsv6630307	copy number variation	74	nstd224	human		GRCh37 chr5: 140,223,194-140,238,124 , GRCh38.p12 chr5: 140,843,609-140,858,539	PCDHA7, PCDHA4, 9 more genes
nsv6629735	copy number variation	1	nstd224	human		GRCh37 chr4: 76,885,365-79,465,559 , GRCh38.p12 chr4: 75,964,212-78,544,405	CCNI, NUP54, 54 more genes
nsv6622479	copy number variation	13	nstd224	human		GRCh37 chr14: 20,213,937-20,425,051 , GRCh38.p12 chr14: 19,745,778-19,956,892	OR4K6P, OR4K5, 11 more genes
nsv6622956	copy number variation	106	nstd224	human		GRCh37 chr15: 22,368,588-22,503,228 , GRCh38.p12 chr15: 22,080,637-22,215,277	IGHV1OR15-4, OR4N4, 9 more genes

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