NA10863 AND nstd20 - dbVar - NCBI

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv438042	copy number variation	6	nstd20	human		NCBI34 chr8: 15,622,969-15,670,924 , GRCh37.p13 chr8: 15,612,603-15,660,558 , GRCh38.p12 chr8: 15,755,094-15,803,049	TUSC3
nsv437950	copy number variation	26	nstd20	human		NCBI34 chr4: 173,669,470-173,686,862 , GRCh37.p13 chr4: 172,973,580-172,990,972 , GRCh38.p12 chr4: 172,052,429-172,069,821	GALNTL6
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
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
nsv437939	copy number variation	19	nstd20	human		NCBI34 chr4: 138,551,715-138,556,685 , GRCh37.p13 chr4: 138,092,894-138,097,864 , GRCh38.p12 chr4: 137,171,740-137,176,710	LINC02511
nsv438137	copy number variation	14	nstd20	human		NCBI34 chr1: 206,205,376-206,209,672 , GRCh37.p13 chr1: 209,121,677-209,125,973 , GRCh38.p12 chr1: 208,948,332-208,952,628	LOC107985255
nsv437887	copy number variation	2	nstd20	human		NCBI34 chr3: 150,285,601-150,288,244 , GRCh37.p13 chr3: 148,964,692-148,967,335 , GRCh38.p12 chr3: 149,246,905-149,249,548	CPHL1P
nsv437925	copy number variation	23	nstd20	human		NCBI34 chr4: 92,391,958-92,393,093 , GRCh37.p13 chr4: 91,933,564-91,934,699 , GRCh38.p12 chr4: 91,012,413-91,013,548	CCSER1
nsv437881	copy number variation	2	nstd20	human		NCBI34 chr3: 131,453,760-131,454,529 , GRCh37.p13 chr3: 130,132,851-130,133,620 , GRCh38.p12 chr3: 130,414,007-130,414,776	COL6A5
nsv438041	copy number variation	6	nstd20	human		GRCh38.p12 chr8: 14,779,255-15,524,673 , NCBI34 chr8: 14,647,130-15,392,548 , GRCh37.p13 chr8: 14,636,764-15,382,182	SGCZ, MIR383
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
nsv438034	copy number variation	6	nstd20	human		GRCh38.p12 chr8: 7,919,727-7,929,431 , NCBI34 chr8: 7,814,659-7,824,363 , GRCh37.p13 chr8: 7,777,249-7,786,953 , GRCh38.p12 chr8\|NT_187570.1: 65,202-74,904	ZNF705G, ZNF705B
nsv437958	copy number variation	4	nstd20	human		GRCh38.p12 chr6: 10,470,804-10,528,561 , NCBI34 chr6: 10,579,023-10,636,780 , GRCh37.p13 chr6: 10,471,037-10,528,794 , GRCh38.p12 chr6\|NW_018654713.1: 1-39,445	GCNT2, LOC100422564, 2 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
nsv437897	copy number variation	5	nstd20	human		NCBI34 chr3: 166,635,288-166,641,054 , GRCh37.p13 chr3: 165,314,375-165,320,141 , GRCh38.p12 chr3: 165,596,587-165,602,353	0
nsv438166	copy number variation	19	nstd20	human		NCBI34 chr10: 20,855,214-20,859,478 , GRCh37.p13 chr10: 20,851,208-20,855,472 , GRCh38.p12 chr10: 20,562,279-20,566,543	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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