NA18991 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
nsv438272	copy number variation	3	nstd20	human		NCBI34 chr17: 15,244,565-15,259,091 , GRCh37.p13 chr17: 15,043,999-15,058,525 , GRCh38.p12 chr17: 15,140,682-15,155,208	LOC107984976
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
nsv437903	copy number variation	23	nstd20	human		NCBI34 chr3: 191,058,267-191,060,542 , GRCh37.p13 chr3: 189,737,354-189,739,629 , GRCh38.p12 chr3: 190,019,565-190,021,840	P3H2
nsv438324	copy number variation	5	nstd20	human		NCBI34 chr22: 16,391,062-16,393,158 , GRCh37.p13 chr22: 18,016,508-18,018,604 , GRCh38.p12 chr22: 17,536,819-17,538,915	CECR2
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
nsv437931	copy number variation	36	nstd20	human		NCBI34 chr4: 115,637,062-115,641,110 , GRCh37.p13 chr4: 115,178,242-115,182,290 , GRCh38.p12 chr4: 114,257,086-114,261,134	0

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