MS23098 AND nstd71 - dbVar - NCBI

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Items: 13

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv886261	copy number variation	152	nstd71	human		NCBI36 chr6: 79,029,920-79,098,352 , GRCh37.p13 chr6: 78,973,201-79,041,633 , GRCh38.p12 chr6: 78,263,484-78,331,916	LOC105377865
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
nsv879310	copy number variation	1929	nstd71	human		NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558	LOC100422402, LOC100132651, 2 more genes
nsv883653	copy number variation	21	nstd71	human		NCBI36 chr6: 29,965,944-29,980,430 , GRCh37.p13 chr6: 29,857,965-29,872,451 , GRCh37.p13 chr6\|NT_167246.1: 1,157,859-1,166,628 , GRCh38.p12 chr6: 29,890,188-29,904,674 , GRCh38.p12 chr6\|NT_167246.2: 1,152,239-1,161,008	HLA-T, HLA-H, 2 more genes
nsv879603	copy number variation	1	nstd71	human		NCBI36 chr4: 93,272,051-93,495,197 , GRCh37.p13 chr4: 93,053,028-93,276,174 , GRCh38.p12 chr4: 92,131,877-92,355,023	GRID2, PMPCAP1, 1 more genes
nsv912000	copy number variation	3	nstd71	human		NCBI36 chr19: 48,160,500-48,333,776 , GRCh37.p13 chr19: 43,468,660-43,641,936 , GRCh38.p12 chr19: 42,964,508-43,137,784	CEACAMP9, PSG11, 2 more genes
nsv872433	copy number variation	1	nstd71	human		NCBI36 chr1: 149,608,041-149,679,804 , GRCh37.p13 chr1: 151,341,417-151,413,180 , GRCh38.p12 chr1: 151,368,941-151,440,704	PSMB4, RNY4P25, 2 more genes
nsv903990	copy number variation	15	nstd71	human		NCBI36 chr15: 32,447,708-32,625,184 , GRCh37.p13 chr15: 34,660,416-34,837,892 , GRCh38.p12 chr15: 34,368,215-34,545,691	ACTG1P15, MIR1233-1, 7 more genes
nsv905949	copy number variation	55	nstd71	human		NCBI36 chr16: 32,406,646-32,511,911 , GRCh37.p13 chr16: 32,499,145-32,604,410 , GRCh38.p12 chr16: 32,487,824-32,593,089	0
nsv873943	copy number variation	269	nstd71	human		NCBI36 chr2: 41,083,802-41,109,046 , GRCh37.p13 chr2: 41,230,298-41,255,542 , GRCh38.p12 chr2: 41,003,158-41,028,402	0
nsv908392	copy number variation	32	nstd71	human		NCBI36 chr17: 41,775,690-42,143,493 , GRCh37.p13 chr17: 44,419,932-44,788,310 , GRCh38.p12 chr17: 46,342,566-46,710,944	LRRC37A2, ARL17B, 6 more genes
nsv884364	copy number variation	2	nstd71	human		NCBI36 chr6: 31,467,172-31,565,157 , GRCh37.p13 chr6\|NT_167249.1: 2,692,980-2,755,239 , GRCh37.p13 chr6: 31,359,193-31,457,178 , GRCh38.p12 chr6: 31,391,416-31,489,401 , GRCh38.p12 chr6\|NT_167249.2: 2,693,682-2,755,941	HCG26, LINC01149, 5 more genes
nsv896727	copy number variation	1	nstd71	human		NCBI36 chr11: 1,637,577-2,043,796 , GRCh37.p13 chr11: 1,681,001-2,087,220 , GRCh38.p12 chr11: 1,659,771-2,065,990	FAM99B, SNORD131, 21 more genes

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