SP51389 AND nstd71 - dbVar - NCBI

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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
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv888900	copy number variation	27	nstd71	human		NCBI36 chr7: 102,032,517-102,062,128 , GRCh37.p13 chr7: 102,245,449-102,274,889 , GRCh38.p12 chr7: 102,605,002-102,634,442	RASA4
nsv909839	copy number variation	966	nstd71	human		NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591	CCDC102B
nsv888728	copy number variation	33	nstd71	human		NCBI36 chr7: 90,020,226-90,065,746 , GRCh37.p13 chr7: 90,182,290-90,227,810 , GRCh38.p12 chr7: 90,552,976-90,598,496	CDK14
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
nsv885203	copy number variation	52	nstd71	human		NCBI36 chr6: 32,616,207-32,629,229 , GRCh37.p13 chr6: 32,508,229-32,521,251 , GRCh38.p12 chr6: 32,540,452-32,553,474	HLA-DRB6, RNU1-61P
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
nsv881874	copy number variation	3	nstd71	human		NCBI36 chr5: 69,326,897-69,428,601 , GRCh37.p13 chr5: 69,291,141-69,392,845 , GRCh38.p12 chr5\|NT_187651.1: 243,313-322,348 , GRCh38.p12 chr5: 69,995,314-70,097,018	NAIPP2, LOC107986372, 4 more genes
nsv882064	copy number variation	28	nstd71	human		NCBI36 chr5: 70,202,676-70,300,876 , GRCh37.p13 chr5: 70,166,920-70,265,120 , GRCh38.p12 chr5: 70,871,093-70,969,293	NAIP, SMN1, 3 more genes
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
nsv885536	copy number variation	17	nstd71	human		NCBI36 chr6: 32,708,781-32,732,638 , GRCh37.p13 chr6\|NT_167249.1: 4,034,248-4,046,862 , GRCh37.p13 chr6\|NT_167246.1: 4,056,958-4,069,536 , GRCh37.p13 chr6: 32,600,803-32,624,660 , GRCh37.p13 chr6\|NT_167247.1: 3,939,666-3,952,277 , GRCh37.p13 chr6\|NT_167245.1: 3,882,525-3,895,103 , GRCh38.p12 chr6\|NT_167247.2: 3,934,081-3,946,695 , GRCh38.p12 chr6\|NT_167245.2: 3,876,940-3,889,518 , GRCh38.p12 chr6: 32,633,026-32,656,883 , GRCh38.p12 chr6\|NT_167249.2: 4,034,950-4,047,564 , GRCh38.p12 chr6\|NT_167246.2: 4,051,338-4,063,916	, , 2 more genes
nsv883891	copy number variation	2	nstd71	human		NCBI36 chr6: 29,984,419-29,999,029 , GRCh37.p13 chr6\|NT_167246.1: 1,170,617-1,185,304 , GRCh37.p13 chr6: 29,876,440-29,891,050 , GRCh38.p12 chr6: 29,908,663-29,923,273 , GRCh38.p12 chr6\|NT_167246.2: 1,164,997-1,179,684	HLA-K, HCG4B, 3 more genes
nsv908379	copy number variation	346	nstd71	human		NCBI36 chr17: 41,775,690-41,922,658 , GRCh37.p13 chr17: 44,419,932-44,566,775 , GRCh38.p12 chr17: 46,342,566-46,489,976	ARL17B, NSFP1, 1 more genes

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