NA18561 AND nstd20 - 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
nsv438038	copy number variation	2	nstd20	human		NCBI34 chr8: 12,556,004-12,565,109 , GRCh37.p13 chr8: 12,545,638-12,554,743 , GRCh38.p12 chr8: 12,688,129-12,697,234	OR7E15P
nsv438271	copy number variation	2	nstd20	human		NCBI34 chr15: 54,508,492-54,511,694 , GRCh37.p13 chr15: 56,792,436-56,795,638 , GRCh38.p12 chr15: 56,500,238-56,503,440
nsv438008	copy number variation	228	nstd20	human		NCBI34 chr7: 141,456,537-141,472,512 , GRCh38.p12 chr7\|NT_187562.1: 311,217-327,170 , GRCh37.p13 chr7\|NW_003571040.1: 491,288-507,241	TRB, TRBV6-2, 2 more genes
nsv438011	copy number variation	95	nstd20	human		NCBI34 chr7: 141,921,685-141,931,471 , GRCh37.p13 chr7: 142,481,301-142,486,383 , GRCh38.p12 chr7\|NT_187562.1: 776,047-785,840 , GRCh37.p13 chr7\|NW_003571040.1: 956,118-965,911	TRB, PRSS3P2, 1 more genes
nsv437921	copy number variation	122	nstd20	human		GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN , NCBI34 chr4: 69,377,786-69,808,237	0
nsv437894	copy number variation	301	nstd20	human		NCBI34 chr3: 163,826,348-163,943,569 , GRCh37.p13 chr3: 162,505,435-162,622,656 , GRCh38.p12 chr3: 162,787,647-162,904,868	0
nsv438337	copy number variation	50	nstd20	human		NCBI34 chr2: 52,726,065-52,757,084 , GRCh37.p13 chr2: 52,751,531-52,782,550 , GRCh38.p12 chr2: 52,524,393-52,555,412	0
nsv437910	copy number variation	98	nstd20	human		NCBI34 chr4: 9,969,524-9,998,131 , GRCh37.p13 chr4: 10,218,641-10,247,248 , GRCh38.p12 chr4: 10,217,017-10,245,624	0
nsv438352	copy number variation	3	nstd20	human		NCBI34 chr2: 59,598,122-59,600,156 , GRCh37.p13 chr2: 59,623,588-59,625,622 , GRCh38.p12 chr2: 59,396,453-59,398,487	0
nsv437868	copy number variation	41	nstd20	human		NCBI34 chr3: 99,731,950-99,732,552 , GRCh37.p13 chr3: 98,411,049-98,411,651 , GRCh38.p12 chr3: 98,692,205-98,692,807	0

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