NA19152 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
nsv438397	copy number variation	9	nstd20	human		NCBI34 chr3: 46,758,432-46,807,284 , GRCh37.p13 chr3: 46,797,840-46,846,692 , GRCh38.p12 chr3: 46,756,350-46,805,202	PRSS43P
nsv438040	copy number variation	13	nstd20	human		NCBI34 chr8: 14,590,534-14,596,692 , GRCh37.p13 chr8: 14,580,168-14,586,326 , GRCh38.p12 chr8: 14,722,659-14,728,817	SGCZ
nsv438126	copy number variation	18	nstd20	human		NCBI34 chr1: 194,080,727-194,081,468 , GRCh37.p13 chr1: 196,792,468-196,793,209 , GRCh38.p12 chr1: 196,823,338-196,824,079	CFHR1
nsv438111	copy number variation	4	nstd20	human		NCBI34 chr9: 102,745,808-102,746,309 , GRCh37.p13 chr9: 107,365,970-107,366,471 , GRCh38.p12 chr9: 104,603,689-104,604,190	OR13C2
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
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
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

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