NA18968 AND nstd20 - 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
nsv438279	copy number variation	3	nstd20	human		NCBI34 chr18: 29,104,106-29,114,504 , GRCh37.p13 chr18: 30,852,119-30,862,517 , GRCh38.p12 chr18: 33,272,155-33,282,553	CCDC178
nsv438207	copy number variation	5	nstd20	human		NCBI34 chr12: 39,168,293-39,169,671 , GRCh37.p13 chr12: 40,882,026-40,883,404 , GRCh38.p12 chr12: 40,488,224-40,489,602	MUC19
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
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
nsv437892	copy number variation	5	nstd20	human		NCBI34 chr3: 163,538,907-163,550,497 , GRCh37.p13 chr3: 162,217,994-162,229,584 , GRCh38.p12 chr3: 162,500,206-162,511,796	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
nsv438369	copy number variation	6	nstd20	human		NCBI34 chr2: 129,734,701-129,735,219 , GRCh37.p13 chr2: 129,641,434-129,641,952 , GRCh38.p12 chr2: 128,883,860-128,884,378	0

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