NA18855 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
nsv437914	copy number variation	20	nstd20	human		NCBI34 chr4: 21,043,096-21,126,700 , GRCh37.p13 chr4: 21,292,213-21,375,817 , GRCh38.p12 chr4: 21,290,590-21,374,194	KCNIP4
nsv438353	copy number variation	6	nstd20	human		NCBI34 chr2: 71,306,841-71,317,129 , GRCh37.p13 chr2: 71,332,303-71,342,591 , GRCh38.p12 chr2: 71,105,173-71,115,461	MCEE
nsv438199	copy number variation	14	nstd20	human		NCBI34 chr12: 27,539,977-27,545,038 , GRCh38.p12 chr12: 27,495,777-27,500,838 , GRCh37.p13 chr12: 27,648,710-27,653,771	SMCO2, RARS1P1
nsv438206	copy number variation	6	nstd20	human		NCBI34 chr12: 39,104,527-39,106,948 , GRCh38.p12 chr12: 40,424,458-40,426,879 , GRCh37.p13 chr12: 40,818,260-40,820,681	MUC19, LOC105369736
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
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
nsv437967	copy number variation	12	nstd20	human		NCBI34 chr6: 33,985,151-33,989,083 , GRCh37.p13 chr6: 33,938,296-33,942,228 , GRCh38.p12 chr6: 33,970,519-33,974,451	0

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