NA19139 AND nstd20 - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv438006	copy number variation	36	nstd20	human		NCBI34 chr7: 133,202,026-133,212,391 , GRCh37.p13 chr7: 133,785,899-133,796,264 , GRCh38.p12 chr7: 134,101,146-134,111,511
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
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
nsv438201	copy number variation	2	nstd20	human		NCBI34 chr12: 32,414,722-32,422,479 , GRCh37.p13 chr12: 32,523,455-32,531,212 , GRCh38.p12 chr12: 32,370,521-32,378,278	BICD1
nsv438375	copy number variation	2	nstd20	human		NCBI34 chr2: 185,330,664-185,336,780 , GRCh37.p13 chr2: 185,128,121-185,134,237 , GRCh38.p12 chr2: 184,263,394-184,269,510	LOC102724340
nsv438033	copy number variation	12	nstd20	human		NCBI34 chr8: 7,201,387-7,206,953 , GRCh37.p13 chr8: 7,213,977-7,219,543 , GRCh38.p12 chr8: 7,356,455-7,362,021	ZNF705G
nsv437889	copy number variation	12	nstd20	human		NCBI34 chr3: 156,501,087-156,505,963 , GRCh37.p13 chr3: 155,180,174-155,185,050 , GRCh38.p12 chr3: 155,462,385-155,467,261	PLCH1
nsv437989	copy number variation	36	nstd20	human		NCBI34 chr7: 89,422,556-89,424,327 , GRCh37.p13 chr7: 89,810,527-89,812,298 , GRCh38.p12 chr7: 90,181,213-90,182,984	STEAP2-AS1
nsv438074	copy number variation	5	nstd20	human		NCBI34 chr8: 103,010,682-103,011,802 , GRCh37.p13 chr8: 103,054,099-103,055,219 , GRCh38.p12 chr8: 102,041,871-102,042,991	NCALD
nsv438194	copy number variation	5	nstd20	human		NCBI34 chr12: 18,371,121-18,458,285 , GRCh38.p12 chr12: 18,326,920-18,414,084 , GRCh37.p13 chr12: 18,479,854-18,567,018	PIK3C2G, NDFIP1P1
nsv438303	copy number variation	4	nstd20	human		NCBI34 chr1: 16,392,736-16,405,381 , GRCh38.p12 chr1: 16,685,160-16,697,805 , GRCh37.p13 chr1: 17,011,655-17,024,300	EIF1AXP1, ESPNP
nsv438229	copy number variation	2	nstd20	human		NCBI34 chr12: 96,379,481-96,391,285 , GRCh38.p12 chr12: 97,483,235-97,495,039 , GRCh37.p13 chr12: 97,877,013-97,888,817	RMST, MIR1251
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
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
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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