MS15610 AND nstd71 - dbVar - NCBI

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Items: 12

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv905668	copy number variation	51	nstd71	human		NCBI36 chr16: 22,627,867-22,696,351 , GRCh37.p13 chr16: 22,720,366-22,788,850 , GRCh38.p12 chr16\|NW_017852933.1: 1,875,186-1,927,115 , GRCh38.p12 chr16: 22,709,045-22,777,529	LOC112268374
nsv890751	copy number variation	169	nstd71	human		NCBI36 chr8: 39,350,791-39,497,557 , GRCh37.p13 chr8: 39,231,634-39,378,400 , GRCh38.p12 chr8: 39,374,115-39,520,881	ADAM5, ADAM3A
nsv893260	copy number variation	21	nstd71	human		NCBI36 chr9: 43,609,749-43,677,629 , GRCh37.p13 chr9: 43,669,753-43,737,633 , GRCh38.p12 chr9: 42,076,756-42,144,636	LOC100420440, CNTNAP3B
nsv911369	copy number variation	219	nstd71	human		NCBI36 chr19: 20,404,485-20,520,617 , GRCh37.p13 chr19: 20,612,645-20,728,777 , GRCh37.p13 chr19\|NW_003571053.2: 347,092-463,224 , GRCh38.p12 chr19: 20,429,839-20,545,971	ZNF737, LOC105372316, 2 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
nsv908545	copy number variation	64	nstd71	human		NCBI36 chr17: 41,995,665-42,092,850 , GRCh37.p13 chr17: 44,640,349-44,737,534 , GRCh38.p12 chr17: 46,562,983-46,660,168	ARL17A, LRRC37A2, 1 more genes
nsv899837	copy number variation	61	nstd71	human		NCBI36 chr13: 18,427,644-18,524,818 , GRCh37.p13 chr13: 19,529,644-19,626,818 , GRCh38.p12 chr13: 18,955,504-19,052,678	USP24P1, PHF2P2, 3 more genes
nsv881429	copy number variation	1	nstd71	human		NCBI36 chr5: 10,194,350-10,342,503 , GRCh37.p13 chr5: 10,141,350-10,289,503 , GRCh38.p12 chr5: 10,141,238-10,289,391	CMBL, ATPSCKMT, 1 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
nsv879254	copy number variation	538	nstd71	human		NCBI36 chr4: 69,047,457-69,179,871 , GRCh37.p13 chr4: 69,364,862-69,497,276 , GRCh38.p12 chr4: 68,499,144-68,631,558	LOC728807, UGT2B29P, 3 more genes
nsv881870	copy number variation	38	nstd71	human		NCBI36 chr5: 69,319,133-69,436,209 , GRCh37.p13 chr5: 69,283,377-69,400,453 , GRCh38.p12 chr5\|NT_187651.1: 243,313-329,959 , GRCh38.p12 chr5: 69,987,550-70,104,626	SMN2, LOC105369228, 5 more genes
nsv906483	copy number variation	1	nstd71	human		NCBI36 chr16: 32,481,352-32,502,614 , GRCh37.p13 chr16: 32,573,851-32,595,113 , GRCh38.p12 chr16: 32,562,530-32,583,792	0

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