IS38294 AND nstd71 - dbVar - NCBI

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv879633	copy number variation	1	nstd71	human		NCBI36 chr4: 97,344,109-97,482,176 , GRCh37.p13 chr4: 97,125,086-97,263,153 , GRCh38.p12 chr4: 96,203,935-96,342,002	LOC100418701, LINC02267
nsv890775	copy number variation	26	nstd71	human		NCBI36 chr8: 39,356,825-39,457,081 , GRCh37.p13 chr8: 39,237,668-39,337,924 , GRCh38.p12 chr8: 39,380,149-39,480,405	ADAM5, ADAM3A
nsv906679	copy number variation	13	nstd71	human		NCBI36 chr16: 54,351,802-54,424,740 , GRCh37.p13 chr16: 55,794,301-55,867,239 , GRCh38.p12 chr16: 55,760,389-55,833,327	CES1, CES1P1
nsv882011	copy number variation	1	nstd71	human		NCBI36 chr5: 70,098,301-70,232,726 , GRCh37.p13 chr5: 70,062,545-70,196,970 , GRCh38.p12 chr5: 70,766,718-70,901,143	SERF1A, CDH12P1, 2 more genes
nsv871709	copy number variation	27	nstd71	human		NCBI36 chr1: 103,904,580-103,966,748 , GRCh37.p13 chr1: 104,103,057-104,165,225 , GRCh38.p12 chr1: 103,560,435-103,622,603	AMY2B, ACTG1P4, 1 more genes
nsv882175	copy number variation	1	nstd71	human		NCBI36 chr5: 70,612,729-70,725,208 , GRCh37.p13 chr5: 70,576,973-70,689,452 , GRCh38.p12 chr5: 71,281,146-71,393,625 , GRCh38.p12 chr5\|NT_187651.1: 811,142-923,604 , GRCh38.p12 chr5\|NW_003315917.2: 1,279,663-1,337,807	, LINC02197, 4 more genes
nsv883671	copy number variation	30	nstd71	human		NCBI36 chr6: 29,965,944-30,003,090 , GRCh37.p13 chr6\|NT_167246.1: 1,157,859-1,189,318 , GRCh37.p13 chr6: 29,857,965-29,895,111 , GRCh38.p12 chr6\|NT_167246.2: 1,152,239-1,183,698 , GRCh38.p12 chr6: 29,890,188-29,927,334	HLA-H, LOC353008, 6 more genes
nsv906242	copy number variation	1	nstd71	human		NCBI36 chr16: 32,439,877-32,504,410 , GRCh37.p13 chr16: 32,532,376-32,596,909 , GRCh38.p12 chr16: 32,521,055-32,585,588	0
nsv879236	copy number variation	1	nstd71	human		NCBI36 chr4: 69,027,229-69,226,833 , GRCh37.p13 chr4: 69,344,634-69,544,238 , GRCh38.p12 chr4: 68,478,916-68,678,520	TMPRSS11E, UGT2B15, 5 more genes
nsv904439	copy number variation	1	nstd71	human		NCBI36 chr15: 79,785,446-79,889,995 , GRCh37.p13 chr15: 81,998,391-82,102,940 , GRCh38.p12 chr15: 81,706,050-81,810,599	0

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