NA19202 AND nstd20 - dbVar - NCBI

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Items: 18

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv438048	copy number variation	78	nstd20	human		NCBI34 chr1: 149,771,758-149,800,260 , GRCh37.p13 chr1: 152,555,176-152,583,678 , GRCh38.p12 chr1: 152,582,700-152,611,202	LCE3C
nsv437930	copy number variation	10	nstd20	human		NCBI34 chr4: 108,651,560-108,665,451 , GRCh37.p13 chr4: 108,192,740-108,206,631 , GRCh38.p12 chr4: 107,271,583-107,285,474	LOC102725220
nsv438379	copy number variation	14	nstd20	human		NCBI34 chr2: 203,499,611-203,511,609 , GRCh37.p13 chr2: 203,297,068-203,309,066 , GRCh38.p12 chr2: 202,432,345-202,444,343	BMPR2
nsv437941	copy number variation	2	nstd20	human		NCBI34 chr4: 144,863,310-144,873,579 , GRCh37.p13 chr4: 144,285,683-144,295,952 , GRCh38.p12 chr4: 143,364,530-143,374,799	GAB1
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
nsv438164	copy number variation	2	nstd20	human		NCBI34 chr10: 11,108,870-11,112,911 , GRCh37.p13 chr10: 11,104,864-11,108,905 , GRCh38.p12 chr10: 11,062,901-11,066,942	CELF2
nsv438053	copy number variation	2	nstd20	human		NCBI34 chr8: 51,082,185-51,083,978 , GRCh37.p13 chr8: 51,032,225-51,034,018 , GRCh38.p12 chr8: 50,119,665-50,121,458	SNTG1
nsv438378	copy number variation	12	nstd20	human		NCBI34 chr2: 196,183,303-196,184,993 , GRCh37.p13 chr2: 195,980,760-195,982,450 , GRCh38.p12 chr2: 195,116,036-195,117,726	LOC105376755
nsv437860	copy number variation	51	nstd20	human		NCBI34 chr1: 72,137,668-72,178,467 , GRCh38.p12 chr1: 72,302,069-72,342,868 , GRCh37.p13 chr1: 72,767,752-72,808,551 , GRCh38.p12 chr1\|NW_018654707.1: 14,336-64,096	RPL31P12, LOC105378797
nsv438245	copy number variation	11	nstd20	human		NCBI34 chr12: 130,625,352-130,630,204 , GRCh38.p12 chr12: 131,646,358-131,651,210 , GRCh37.p13 chr12: 132,130,903-132,135,755	LINC02414, LOC105370086
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
nsv438171	copy number variation	2	nstd20	human		GRCh38.p12 chr10: 46,591,001-46,606,239 , NCBI34 chr10: 46,327,384-46,342,622 , GRCh37.p13 chr10: 46,943,378-46,958,616 , GRCh37.p13 chr10\|NW_003871068.1: 862,116-877,354	SYT15, SYT15-AS1, 1 more genes
nsv437962	copy number variation	7	nstd20	human		NCBI34 chr6: 29,961,770-30,000,151 , GRCh37.p13 chr6\|NT_113891.2: 1,369,681-1,408,031 , GRCh37.p13 chr6\|NT_167245.1: 1,150,955-1,189,313 , GRCh37.p13 chr6\|NT_167247.1: 1,150,592-1,177,759 , GRCh37.p13 chr6\|NT_167248.1: 1,150,632-1,188,959 , GRCh37.p13 chr6\|NT_167249.1: 1,187,290-1,225,562 , GRCh37.p13 chr6\|NT_167244.1: 1,097,817-1,136,167 , GRCh37.p13 chr6\|NT_167246.1: 1,150,228-1,188,558 , GRCh37.p13 chr6\|NW_003871063.1: 124,078-162,428 , GRCh37.p13 chr6: 29,855,945-29,894,351 , GRCh38.p12 chr6: 29,905,621-29,926,574 , GRCh38.p12 chr6\|NT_167247.2: 1,145,007-1,172,174 , GRCh38.p12 chr6\|NT_167248.2: 1,145,036-1,183,363 , GRCh38.p12 chr6\|NT_167249.2: 1,187,992-1,226,264 , GRCh38.p12 chr6\|NT_167245.2: 1,145,370-1,183,728 , GRCh38.p12 chr6\|NT_113891.3: 1,387,004-1,407,925 , GRCh38.p12 chr6\|NT_167246.2: 1,144,608-1,182,938 , GRCh38.p12 chr6\|NT_167244.2: 1,147,901-1,186,251	HLA-A, HLA-H, 7 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
nsv437996	copy number variation	57	nstd20	human		NCBI34 chr7: 109,002,325-109,011,761 , GRCh37.p13 chr7: 109,441,794-109,451,230 , GRCh38.p12 chr7: 109,801,737-109,811,173	0
nsv437964	copy number variation	6	nstd20	human		NCBI34 chr6: 31,382,098-31,387,190 , GRCh37.p13 chr6\|NT_113891.2: 2,790,607-2,795,699 , GRCh37.p13 chr6\|NT_167247.1: 2,657,879-2,662,962 , GRCh37.p13 chr6\|NT_167248.1: 2,570,878-2,575,945 , GRCh37.p13 chr6\|NT_167249.1: 2,611,106-2,616,172 , GRCh37.p13 chr6\|NT_167246.1: 2,624,194-2,629,281 , GRCh37.p13 chr6: 31,277,368-31,282,462 , GRCh38.p12 chr6: 31,309,591-31,314,685 , GRCh38.p12 chr6\|NT_167247.2: 2,652,294-2,657,377 , GRCh38.p12 chr6\|NT_167248.2: 2,565,282-2,570,349 , GRCh38.p12 chr6\|NT_167249.2: 2,611,808-2,616,874 , GRCh38.p12 chr6\|NT_113891.3: 2,790,501-2,795,593 , GRCh38.p12 chr6\|NT_167246.2: 2,618,574-2,623,661	0
nsv438197	copy number variation	6	nstd20	human		NCBI34 chr12: 22,139,915-22,142,636 , GRCh37.p13 chr12: 22,248,648-22,251,369 , GRCh38.p12 chr12: 22,095,714-22,098,435	0
nsv438257	copy number variation	2	nstd20	human		NCBI34 chr13: 95,875,940-95,876,926 , GRCh37.p13 chr13: 98,177,939-98,178,925 , GRCh38.p12 chr13: 97,525,685-97,526,671	0

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