NA12005 AND nstd20 - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv438123	copy number variation	4	nstd20	human		NCBI34 chrX: 11,381,612-11,410,075 , GRCh37.p13 chrX: 12,020,186-12,048,649 , GRCh38.p12 chrX: 12,002,067-12,030,530	FRMPD4
nsv437987	copy number variation	1	nstd20	human		NCBI34 chr7: 75,913,423-75,923,509 , GRCh37.p13 chr7: 76,301,334-76,311,420 , GRCh38.p12 chr7: 76,672,017-76,682,103 , GRCh38.p12 chr7\|NT_187561.1: 158,852-168,938
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
nsv438050	copy number variation	126	nstd20	human		GRCh38.p12 chr8: 39,375,220-39,536,536 , NCBI34 chr8: 39,250,107-39,411,423 , GRCh37.p13 chr8: 39,232,739-39,394,055	ADAM3A, ADAM5
nsv438331	copy number variation	6	nstd20	human		NCBI34 chr22: 20,779,134-20,808,466 , GRCh38.p12 chr22: 22,100,170-22,129,518 , GRCh37.p13 chr22: 22,454,580-22,483,912	IGL, ABHD17AP5, 1 more genes
nsv438338	copy number variation	81	nstd20	human		NCBI34 chr22: 21,026,944-21,558,650 , GRCh37.p13 chr22: 22,702,390-23,234,096 , GRCh38.p12 chr22: 22,348,040-22,891,916	BCRP4, IGL, 72 more genes
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
nsv438361	copy number variation	15	nstd20	human		NCBI34 chr2: 89,093,935-89,175,498 , GRCh37.p13 chr2: 89,191,791-89,273,354 , GRCh38.p12 chr2: 88,892,275-88,973,835 , GRCh38.p12 chr2\|NW_012132915.1: 1,101-82,661	IGKV1-5, IGKV7-3, 8 more genes
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
nsv438230	copy number variation	4	nstd20	human		NCBI34 chr12: 96,517,213-96,533,447 , GRCh37.p13 chr12: 98,014,745-98,030,979 , GRCh38.p12 chr12: 97,620,967-97,637,201	0
nsv438046	copy number variation	39	nstd20	human		NCBI34 chr8: 24,996,369-25,011,464 , GRCh37.p13 chr8: 24,974,459-24,989,554 , GRCh38.p12 chr8: 25,116,944-25,132,039	0
nsv438360	copy number variation	17	nstd20	human		NCBI34 chr2: 89,039,268-89,049,267 , GRCh37.p13 chr2: 89,137,124-89,147,123 , GRCh38.p12 chr2: 88,837,611-88,847,610	0
nsv438292	copy number variation	16	nstd20	human		NCBI34 chr2: 34,688,262-34,696,094 , GRCh37.p13 chr2: 34,713,727-34,721,559 , GRCh38.p12 chr2: 34,488,660-34,496,492	0
nsv437929	copy number variation	2	nstd20	human		NCBI34 chr4: 105,212,443-105,219,862 , GRCh37.p13 chr4: 104,753,623-104,761,042 , GRCh38.p12 chr4: 103,832,466-103,839,885	0
nsv438005	copy number variation	72	nstd20	human		NCBI34 chr7: 125,601,054-125,603,762 , GRCh37.p13 chr7: 126,046,565-126,049,273 , GRCh38.p12 chr7: 126,406,511-126,409,219	0
nsv437954	copy number variation	2	nstd20	human		NCBI34 chr5: 109,500,767-109,501,608 , GRCh37.p13 chr5: 109,424,551-109,425,392 , GRCh38.p12 chr5: 110,088,850-110,089,691	0

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