HGDP00885 AND nstd27 - dbVar - NCBI

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Items: 9

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv463200	copy number variation	1	nstd27	human		NCBI35 chr6: 79,022,244-79,088,461 , GRCh37.p13 chr6: 78,965,525-79,031,742 , GRCh38.p12 chr6: 78,255,808-78,322,025	LOC105377865
nsv464788	copy number variation	1	nstd27	human		NCBI35 chr7: 141,213,982-141,247,974 , GRCh37.p13 chr7\|NW_003571040.1: 202,949-236,941 , GRCh37.p13 chr7: 141,760,798-141,794,790 , GRCh38.p12 chr7: 142,060,998-142,094,990 , GRCh38.p12 chr7\|NT_187562.1: 22,878-56,870	MGAM
nsv466072	copy number variation	1	nstd27	human		NCBI35 chr1: 172,162,512-172,470,660 , GRCh37.p13 chr1: 175,430,855-175,739,003 , GRCh38.p12 chr1: 175,461,719-175,769,867	TNR
nsv464423	copy number variation	1	nstd27	human		NCBI35 chr7: 32,904,969-32,966,040 , GRCh37.p13 chr7: 33,131,729-33,192,800 , GRCh38.p12 chr7: 33,092,117-33,153,188	RP9, BBS9
nsv457622	copy number variation	1	nstd27	human		NCBI35 chr16: 87,801,384-87,913,062 , GRCh37.p13 chr16: 89,273,883-89,385,561 , GRCh38.p12 chr16: 89,207,475-89,319,153	LOC105371414, LOC100287036, 3 more genes
nsv458449	copy number variation	1	nstd27	human		NCBI35 chr19: 20,422,200-20,507,201 , GRCh37.p13 chr19\|NW_003571053.2: 364,807-449,808 , GRCh37.p13 chr19: 20,630,360-20,715,361 , GRCh38.p12 chr19: 20,447,554-20,532,555	ZNF737, LOC105372317, 1 more genes
nsv456600	copy number variation	1	nstd27	human		NCBI35 chr14: 106,174,317-106,243,464 , GRCh37.p13 chr14: 107,103,272-107,172,419 , GRCh38.p12 chr14: 106,647,269-106,717,172	IGHV3-64, IGHVII-65-1, 15 more genes
nsv456350	copy number variation	1	nstd27	human		NCBI35 chr14: 82,636,173-84,440,848 , GRCh37.p13 chr14: 83,566,420-85,371,095 , GRCh38.p12 chr14: 83,100,076-84,904,751	LINC02305, LOC105370601, 6 more genes
nsv466961	copy number variation	1	nstd27	human		NCBI35 chr1: 188,160,138-188,237,630 , GRCh37.p13 chr1: 191,428,481-191,505,973 , GRCh38.p12 chr1: 191,459,351-191,536,843	0

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