HGDP00088 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
nsv457538	copy number variation	1	nstd27	human		NCBI35 chr16: 74,988,028-75,010,544 , GRCh37.p13 chr16: 76,430,527-76,453,043 , GRCh38.p12 chr16: 76,396,630-76,419,146	CNTNAP4
nsv460838	copy number variation	1	nstd27	human		NCBI35 chr3: 124,935,528-124,946,398 , GRCh37.p13 chr3: 123,452,838-123,463,708 , GRCh38.p12 chr3: 123,733,991-123,744,861	MYLK
nsv461267	copy number variation	1	nstd27	human		NCBI35 chr4: 10,551,202-10,946,148 , GRCh37.p13 chr4: 10,874,933-11,269,879 , GRCh38.p12 chr4: 10,873,309-11,268,255	LOC105374488
nsv460854	copy number variation	1	nstd27	human		NCBI35 chr3: 131,660,438-131,722,422 , GRCh37.p13 chr3: 130,177,740-130,239,724 , GRCh38.p12 chr3: 130,458,896-130,520,880	COL6A6, COL6A5
nsv466772	copy number variation	1	nstd27	human		NCBI35 chr1: 187,177,910-187,223,937 , GRCh37.p13 chr1: 190,446,253-190,492,280 , GRCh38.p12 chr1: 190,477,123-190,523,150	BRINP3, BRINP3-DT
nsv467903	copy number variation	1	nstd27	human		NCBI35 chr11: 55,127,597-55,198,944 , GRCh37.p13 chr11: 55,371,021-55,442,368 , GRCh38.p12 chr11: 55,603,545-55,674,892	OR4V1P, OR4C11, 3 more genes
nsv461641	copy number variation	1	nstd27	human		NCBI35 chr4: 131,897,623-131,947,025 , GRCh37.p13 chr4: 131,540,018-131,589,420 , GRCh38.p12 chr4: 130,618,863-130,668,265	0
nsv462088	copy number variation	1	nstd27	human		NCBI35 chr5: 30,942,738-30,969,332 , GRCh37.p13 chr5: 30,906,981-30,933,575 , GRCh38.p12 chr5: 30,906,874-30,933,468	0
nsv469196	copy number variation	1	nstd27	human		NCBI35 chr12: 31,101,381-31,298,174 , GRCh37.p13 chr12: 31,210,114-31,406,907 , GRCh38.p12 chr12: 31,057,180-31,253,973 , GRCh38.p12 chr12\|NT_187587.1: 1-144,767	DDX11, OVOS2, 8 more genes

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