IS34443 AND nstd71 - dbVar - NCBI

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Items: 11

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv890803	copy number variation	10	nstd71	human		NCBI36 chr8: 39,379,684-39,509,376 , GRCh37.p13 chr8: 39,260,527-39,390,219 , GRCh38.p12 chr8: 39,403,008-39,532,700	ADAM3A, ADAM5
nsv900397	copy number variation	62	nstd71	human		NCBI36 chr13: 65,993,886-66,078,046 , GRCh37.p13 chr13: 67,095,885-67,180,045 , GRCh38.p12 chr13: 66,521,753-66,605,913	LOC105370247, PCDH9
nsv885155	copy number variation	9	nstd71	human		NCBI36 chr6: 32,611,857-32,635,057 , GRCh37.p13 chr6: 32,503,879-32,527,079 , GRCh38.p12 chr6: 32,536,102-32,559,302	HLA-DRB6, RNU1-61P
nsv881881	copy number variation	16	nstd71	human		NCBI36 chr5: 69,331,520-69,436,209 , GRCh37.p13 chr5: 69,295,764-69,400,453 , GRCh38.p12 chr5\|NT_187651.1: 243,313-329,959 , GRCh38.p12 chr5: 69,999,937-70,104,626	LOC107986372, NAIPP2, 3 more genes
nsv882084	copy number variation	25	nstd71	human		NCBI36 chr5: 70,232,726-70,300,876 , GRCh37.p13 chr5: 70,196,970-70,265,120 , GRCh38.p12 chr5: 70,901,143-70,969,293	SERF1A, NAIP, 2 more genes
nsv896537	copy number variation	7	nstd71	human		NCBI36 chr11: 402,449-444,363 , GRCh37.p13 chr11: 412,449-454,363 , GRCh38.p12 chr11: 412,449-454,363	LOC105376506, SIGIRR, 3 more genes
nsv893216	copy number variation	1	nstd71	human		NCBI36 chr9: 43,559,955-43,683,382 , GRCh37.p13 chr9: 43,619,959-43,743,386 , GRCh38.p12 chr9: 42,071,003-42,194,430	CNTNAP3B, PTS-P1, 2 more genes
nsv899655	copy number variation	1	nstd71	human		NCBI36 chr12: 130,294,704-130,395,261 , GRCh37.p13 chr12: 131,728,751-131,829,308 , GRCh38.p12 chr12: 131,244,206-131,344,763	, LINC02415, 5 more genes
nsv886198	copy number variation	304	nstd71	human		NCBI36 chr6: 77,073,066-77,088,077 , GRCh37.p13 chr6: 77,016,346-77,031,357 , GRCh38.p12 chr6: 76,306,629-76,321,640	0
nsv903312	copy number variation	16	nstd71	human		NCBI36 chr15: 19,788,495-20,080,112 , GRCh37.p13 chr15: 22,287,131-22,578,748 , GRCh38.p12 chr15: 21,999,180-22,290,797	OR11K1P, OR4N3P, 17 more genes
nsv902511	copy number variation	3	nstd71	human		NCBI36 chr14: 105,080,617-105,308,150 , GRCh37.p13 chr14: 106,009,572-106,237,105 , GRCh37.p13 chr14\|NW_004166863.1: 206,402-433,935 , GRCh38.p12 chr14\|NT_187600.1: 10,233-238,537 , GRCh38.p12 chr14: 105,543,235-105,770,768	, IGH, 19 more genes

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