MS14978 AND nstd71 - dbVar - NCBI

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Items: 17

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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
nsv889263	copy number variation	249	nstd71	human		NCBI36 chr7: 141,410,335-141,441,259 , GRCh37.p13 chr7\|NW_003571040.1: 206,017-236,941 , GRCh37.p13 chr7: 141,763,866-141,794,790 , GRCh38.p12 chr7: 142,064,066-142,094,990 , GRCh38.p12 chr7\|NT_187562.1: 25,946-56,870	MGAM
nsv890754	copy number variation	920	nstd71	human		NCBI36 chr8: 39,350,791-39,509,376 , GRCh37.p13 chr8: 39,231,634-39,390,219 , GRCh38.p12 chr8: 39,374,115-39,532,700	ADAM5, ADAM3A
nsv908473	copy number variation	144	nstd71	human		NCBI36 chr17: 41,801,275-41,922,658 , GRCh37.p13 chr17: 44,445,525-44,566,775 , GRCh38.p12 chr17: 46,368,159-46,489,976 , GRCh38.p12 chr17\|NT_187663.1: 1,118,390-1,181,521	NSF, NSFP1
nsv903647	copy number variation	13	nstd71	human		NCBI36 chr15: 21,985,041-22,096,612 , GRCh37.p13 chr15: 24,433,948-24,545,519 , GRCh38.p12 chr15: 24,188,801-24,300,372	LOC105370733, LOC105370732
nsv893234	copy number variation	15	nstd71	human		NCBI36 chr9: 43,594,114-43,683,382 , GRCh37.p13 chr9: 43,654,118-43,743,386 , GRCh38.p12 chr9: 42,071,003-42,160,271	CNTNAP3B, LOC100420440
nsv871196	copy number variation	88	nstd71	human		NCBI36 chr1: 12,777,429-12,810,136 , GRCh37.p13 chr1: 12,854,842-12,887,549 , GRCh38.p12 chr1: 12,794,693-12,827,690	PRAMEF11, PRAMEF1, 1 more genes
nsv883869	copy number variation	6	nstd71	human		NCBI36 chr6: 29,982,594-29,992,880 , GRCh37.p13 chr6\|NT_167246.1: 1,168,792-1,179,076 , GRCh37.p13 chr6: 29,874,615-29,884,901 , GRCh38.p12 chr6\|NT_167246.2: 1,163,172-1,173,456 , GRCh38.p12 chr6: 29,906,838-29,917,124	DDX39BP1, MCCD1P1, 2 more genes
nsv873423	copy number variation	1	nstd71	human		NCBI36 chr1: 244,990,484-245,045,127 , GRCh37.p13 chr1: 246,923,861-246,978,504 , GRCh38.p12 chr1: 246,760,559-246,815,202	KIF28P, LINC01341, 2 more genes
nsv888447	copy number variation	5	nstd71	human		NCBI36 chr7: 76,038,186-76,411,221 , GRCh37.p13 chr7: 76,200,250-76,573,285 , GRCh38.p12 chr7: 76,570,933-76,943,968	POMZP3, , 4 more genes
nsv902761	copy number variation	101	nstd71	human		NCBI36 chr15: 19,031,743-19,212,282 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr15: 20,729,748-21,258,351	POTEB2, MIR5701-1, 22 more genes
nsv905940	copy number variation	1	nstd71	human		NCBI36 chr16: 32,406,646-32,450,736 , GRCh37.p13 chr16: 32,499,145-32,543,235 , GRCh38.p12 chr16: 32,487,824-32,531,914	0
nsv906417	copy number variation	125	nstd71	human		NCBI36 chr16: 32,469,358-32,511,911 , GRCh37.p13 chr16: 32,561,857-32,604,410 , GRCh38.p12 chr16: 32,550,536-32,593,089	0
nsv884226	copy number variation	67	nstd71	human		NCBI36 chr6: 31,385,967-31,396,472 , GRCh37.p13 chr6: 31,277,988-31,288,493 , GRCh37.p13 chr6\|NT_167249.1: 2,611,726-2,622,207 , GRCh37.p13 chr6\|NT_167246.1: 2,624,814-2,631,393 , GRCh38.p12 chr6\|NT_167246.2: 2,619,194-2,625,775 , GRCh38.p12 chr6\|NT_167249.2: 2,612,428-2,622,909 , GRCh38.p12 chr6: 31,310,211-31,320,716	0
nsv903213	copy number variation	198	nstd71	human		NCBI36 chr15: 19,635,853-19,950,423 , GRCh37.p13 chr15: 21,371,194-22,449,059 , GRCh38.p12 chr15: 21,165,865-22,161,108	OR4H6P, OR4Q1P, 49 more genes
nsv903123	copy number variation	6	nstd71	human		NCBI36 chr15: 19,372,096-19,556,128 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr15: 20,924,655-21,498,353	FAM30C, LONRF2P4, 23 more genes
nsv890242	copy number variation	1	nstd71	human		NCBI36 chr8: 7,342,465-7,830,417 , GRCh37.p13 chr8: 7,355,055-7,793,007 , GRCh38.p12 chr8: 7,497,533-7,935,485 , GRCh38.p12 chr8\|NW_018654717.1: 5,267,605-5,513,617	FAM90A21P, FAM90A10, 46 more genes
nsv873424	copy number variation	1	nstd71	human		NCBI36 chr1: 245,057,717-245,433,003 , GRCh37.p13 chr1: 246,991,094-247,366,380 , GRCh38.p12 chr1: 246,827,792-247,203,078	RNA5SP82, LOC100420880, 15 more genes

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MS14978 AND nstd71 (18)
dbVar
glycosyl hydrolase [Streptococcus sp. HMSC061D10]
glycosyl hydrolase [Streptococcus sp. HMSC061D10]
gi|1080605211|gb|OFN81645.1||gnl|WG V|HMPREF2728_00665

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