SP52332 AND nstd71 - dbVar - NCBI

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Number of Variants: 8

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv897949	copy number variation	2	nstd71	human		NCBI36 chr11: 78,499,593-78,575,110 , GRCh37.p13 chr11: 78,821,945-78,897,462 , GRCh38.p12 chr11: 79,110,900-79,186,417	TENM4
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
nsv887075	copy number variation	152	nstd71	human		NCBI36 chr7: 136,005-176,320 , GRCh37.p13 chr7: 40,922-81,237 , GRCh38.p12 chr7: 43,902-81,237 , GRCh38.p12 chr7\|NT_187558.1: 1-37,336 , GRCh38.p12 chr7\|NT_187653.1: 36,223-73,558	LOC101929756, LOC105375113
nsv911912	copy number variation	43	nstd71	human		NCBI36 chr19: 48,060,801-48,160,500 , GRCh37.p13 chr19: 43,368,961-43,468,660 , GRCh38.p12 chr19: 42,864,809-42,964,508	CEACAMP7, PSG1, 2 more genes
nsv883485	copy number variation	2	nstd71	human		NCBI36 chr6: 25,367,116-25,545,965 , GRCh37.p13 chr6: 25,259,137-25,437,986 , GRCh38.p12 chr6: 25,258,909-25,437,758	CARMIL1, RPL21P68, 2 more genes
nsv911729	copy number variation	1	nstd71	human		NCBI36 chr19: 46,013,212-46,075,668 , GRCh37.p13 chr19: 41,321,372-41,383,828 , GRCh38.p12 chr19: 40,815,467-40,877,923	CYP2F2P, CYP2A7, 1 more genes
nsv896967	copy number variation	31	nstd71	human		NCBI36 chr11: 5,858,528-5,911,385 , GRCh37.p13 chr11: 5,901,952-5,954,809 , GRCh38.p12 chr11: 5,880,722-5,933,579	LOC112268071, OR52E4, 2 more genes
nsv906417	copy number variation	125	nstd71	human		NCBI36 chr16: 32,469,358-32,511,911 , GRCh37.p13 chr16: 32,561,857-32,604,410 , GRCh38.p12 chr16: 32,550,536-32,593,089	0

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