M2505 AND nstd157 - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3317594	copy number variation	18	nstd157	human		GRCh37 chr1: 245,636,915-245,647,809 , GRCh38.p12 chr1: 245,473,613-245,484,507 , GRCh38.p12 chr1\|NT_187516.1: 167,917-178,811	KIF26B
nsv3317857	copy number variation	22	nstd157	human		GRCh37 chr15: 56,789,979-56,800,635 , GRCh38.p12 chr15: 56,497,781-56,508,437
nsv3318953	copy number variation	35	nstd157	human		GRCh37 chr3: 53,032,639-53,038,786 , GRCh38.p12 chr3: 52,998,623-53,004,770	SFMBT1
nsv3317990	copy number variation	1	nstd157	human		GRCh37 chr6: 124,543,314-124,565,222 , GRCh38.p12 chr6: 124,222,168-124,244,076	NKAIN2
nsv3317623	copy number variation	1	nstd157	human		GRCh37 chr5: 156,531,114-156,536,307 , GRCh38.p12 chr5: 157,104,103-157,109,296	HAVCR2
nsv3318924	copy number variation	14	nstd157	human		GRCh38.p12 chr15: 97,271,952-97,288,602 , GRCh37 chr15: 97,815,182-97,831,832	LOC105371006, LINC02253
nsv3317440	copy number variation	2	nstd157	human		GRCh38.p12 chr16: 2,923,248-2,935,683 , GRCh37 chr16: 2,973,249-2,985,684	FLYWCH1, RPL23AP86
nsv3318690	copy number variation	14	nstd157	human		GRCh38.p12 chr2: 38,733,349-38,744,481 , GRCh37 chr2: 38,960,491-38,971,623	SRSF7, GALM
nsv3318379	copy number variation	4	nstd157	human		GRCh37 chr3: 100,340,145-100,439,759 , GRCh38.p12 chr3: 100,621,301-100,720,915	TFG, ADGRG7, 1 more genes
nsv3317336	copy number variation	2	nstd157	human		GRCh37 chr7: 65,414,031-65,464,524 , GRCh38.p12 chr7: 65,949,044-65,999,537	GUSB, VKORC1L1, 1 more genes
nsv3317327	copy number variation	24	nstd157	human		GRCh38.p12 chr2: 241,911,938-242,092,368 , GRCh37 chr2: 242,854,089-243,034,519 , GRCh38.p12 chr2\|NT_187647.1: 1-136,078 , GRCh38.p12 chr2\|NT_187523.1: 1-136,438	LOC285097, LINC01881, 4 more genes
nsv3317861	copy number variation	37	nstd157	human		GRCh37 chr6: 67,011,900-67,048,885 , GRCh38.p12 chr6: 66,302,007-66,338,992	0
nsv3318230	copy number variation	25	nstd157	human		GRCh37 chr2: 184,795,725-184,803,456 , GRCh38.p12 chr2: 183,930,998-183,938,729	0
nsv3318502	copy number variation	31	nstd157	human		GRCh37 chr9: 78,004,378-78,011,616 , GRCh38.p12 chr9: 75,389,462-75,396,700	0
nsv3318671	copy number variation	17	nstd157	human		GRCh37 chr5: 180,176,005-180,195,526 , GRCh38.p12 chr5: 180,749,005-180,768,526	0

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