SP53972 AND nstd71 - dbVar - NCBI

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv905543	copy number variation	10	nstd71	human		NCBI36 chr16: 18,482,284-18,687,337 , GRCh37.p13 chr16: 18,574,783-18,779,836 , GRCh38.p12 chr16: 18,563,461-18,768,514	ABCC6P1
nsv886250	copy number variation	523	nstd71	human		NCBI36 chr6: 79,022,244-79,098,352 , GRCh37.p13 chr6: 78,965,525-79,041,633 , GRCh38.p12 chr6: 78,255,808-78,331,916	LOC105377865
nsv884818	copy number variation	499	nstd71	human		NCBI36 chr6: 32,560,168-32,591,507 , GRCh37.p13 chr6: 32,452,190-32,483,529 , GRCh38.p12 chr6: 32,484,413-32,515,752	HLA-DRB5
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
nsv890818	copy number variation	41	nstd71	human		NCBI36 chr8: 39,428,327-39,497,557 , GRCh37.p13 chr8: 39,309,170-39,378,400 , GRCh38.p12 chr8: 39,451,651-39,520,881	ADAM3A
nsv897418	copy number variation	15	nstd71	human		NCBI36 chr11: 48,886,497-48,911,330 , GRCh37.p13 chr11: 48,929,921-48,954,754 , GRCh38.p12 chr11: 48,908,369-48,933,202	LOC100420449
nsv893264	copy number variation	10	nstd71	human		NCBI36 chr9: 43,609,749-43,720,352 , GRCh37.p13 chr9: 43,669,753-43,780,356 , GRCh38.p12 chr9: 42,034,033-42,144,636	CNTNAP3B, LOC100420440
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
nsv902782	copy number variation	16	nstd71	human		NCBI36 chr15: 19,031,743-19,494,732 , GRCh37.p13 chr15: 20,771,729-22,141,158 , GRCh38.p12 chr15: 20,566,406-21,498,353	RNU6-749P, LOC283804, 39 more genes
nsv881164	copy number variation	59	nstd71	human		NCBI36 chr5: 28,672,109-28,767,883 , GRCh37.p13 chr5: 28,636,352-28,732,126 , GRCh38.p12 chr5: 28,636,245-28,732,019	0
nsv895538	copy number variation	101	nstd71	human		NCBI36 chr10: 58,562,281-58,608,558 , GRCh37.p13 chr10: 58,892,275-58,938,552 , GRCh38.p12 chr10: 57,132,515-57,178,792	0
nsv908523	copy number variation	4	nstd71	human		NCBI36 chr17: 41,854,987-41,922,658 , GRCh37.p13 chr17\|NT_167251.1: 263,369-308,670 , GRCh37.p13 chr17: 44,499,551-44,566,775 , GRCh38.p12 chr17: 46,444,391-46,489,976	0
nsv906010	copy number variation	2	nstd71	human		NCBI36 chr16: 32,413,490-32,436,693 , GRCh37.p13 chr16: 32,505,989-32,529,192 , GRCh38.p12 chr16: 32,494,668-32,517,871	0
nsv914701	copy number variation	14	nstd71	human		NCBI36 chr22: 23,991,725-24,234,257 , GRCh37.p13 chr22: 25,661,725-25,904,257 , GRCh38.p12 chr22: 25,265,758-25,508,290	LOC100419673, LOC105372969, 4 more genes
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
nsv906362	copy number variation	3	nstd71	human		NCBI36 chr16: 32,465,671-32,511,911 , GRCh37.p13 chr16: 32,558,170-32,604,410 , GRCh38.p12 chr16: 32,546,849-32,593,089	0

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SP53972 AND nstd71 (17)
dbVar
SP58077 AND nstd71 (9)
dbVar
PREDICTED: Homo sapiens copine 3 (CPNE3), transcript variant X3, mRNA
PREDICTED: Homo sapiens copine 3 (CPNE3), transcript variant X3, mRNA
gi|2462621509|ref|XM_054361450.1|

Nucleotide

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