NA18632 AND nstd20 - dbVar - NCBI

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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
nsv438014	copy number variation	27	nstd20	human		NCBI34 chr8: 534,755-588,391 , GRCh37.p13 chr8: 544,755-598,391 , GRCh38.p12 chr8: 594,755-648,391	ERICH1
nsv437950	copy number variation	26	nstd20	human		NCBI34 chr4: 173,669,470-173,686,862 , GRCh37.p13 chr4: 172,973,580-172,990,972 , GRCh38.p12 chr4: 172,052,429-172,069,821	GALNTL6
nsv437997	copy number variation	8	nstd20	human		NCBI34 chr7: 109,735,375-109,745,762 , GRCh37.p13 chr7: 110,174,844-110,185,231 , GRCh38.p12 chr7: 110,534,787-110,545,174	LOC105375451
nsv437907	copy number variation	146	nstd20	human		NCBI34 chr3: 194,196,286-194,205,086 , GRCh37.p13 chr3: 192,875,373-192,884,173 , GRCh38.p12 chr3: 193,157,584-193,166,384	VEZF1P1
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
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
nsv438133	copy number variation	1	nstd20	human		NCBI34 chrX: 57,162,074-57,167,037 , GRCh37.p13 chrX: 58,195,283-58,200,246 , GRCh38.p12 chrX: 58,168,849-58,173,812	0
nsv438052	copy number variation	1	nstd20	human		NCBI34 chr8: 41,124,713-41,125,490 , GRCh37.p13 chr8: 41,107,345-41,108,122 , GRCh38.p12 chr8: 41,249,826-41,250,603	0

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