1-0912-004 AND nstd173 - 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
nsv4385917	copy number variation	155	nstd173	human		GRCh37 chr2: 98,138,417-98,162,188 , GRCh38.p12 chr2: 97,521,954-97,545,725	ANKRD36B
nsv4387053	copy number variation	81	nstd173	human		GRCh37 chr6: 124,432,055-124,470,365 , GRCh38.p12 chr6: 124,110,910-124,149,220	NKAIN2
nsv4370230	copy number variation	1	nstd173	human		GRCh37 chr5: 86,472,349-86,493,926 , GRCh38.p12 chr5: 87,176,532-87,198,109	LOC101929380
nsv4375212	copy number variation	547	nstd173	human		GRCh37 chr1: 72,762,663-72,811,904 , GRCh38.p12 chr1: 72,296,980-72,346,221 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,446	RPL31P12, LOC105378797
nsv4367574	copy number variation	2	nstd173	human		GRCh37 chr10: 128,766,925-128,905,820 , GRCh38.p12 chr10: 126,968,661-127,107,556	DOCK1, LOC105378552, 1 more genes
nsv4385047	copy number variation	40	nstd173	human		GRCh37 chr4: 69,435,889-69,544,335 , GRCh38.p12 chr4: 68,570,171-68,678,617	UGT2B15, LOC728807, 3 more genes
nsv4379490	copy number variation	34	nstd173	human		GRCh37 chr11: 55,376,649-55,442,305 , GRCh38.p12 chr11: 55,609,173-55,674,829	OR4C6, OR4S2, 2 more genes
nsv4370277	copy number variation	687	nstd173	human		GRCh37 chr5: 180,378,754-180,430,789 , GRCh38.p12 chr5: 180,951,754-181,003,789	BTNL8, ARPP19P1, 3 more genes
nsv4385198	copy number variation	25	nstd173	human		GRCh37 chr14: 45,173,899-45,226,859 , GRCh38.p12 chr14: 44,704,696-44,757,656	0
nsv4378809	copy number variation	20	nstd173	human		GRCh37 chr5: 140,218,726-140,253,787 , GRCh38.p12 chr5: 140,839,141-140,874,202	PCDHA7, PCDHA4, 13 more genes
nsv4387464	copy number variation	23	nstd173	human		GRCh37 chr12: 31,355,873-31,407,123 , GRCh38.p12 chr12: 31,202,939-31,254,189 , GRCh38.p12 chr12\|NT_187587.1: 93,733-144,983	MTCYBP26, RPL13AP22, 4 more genes
nsv4385415	copy number variation	63	nstd173	human		GRCh37 chr17: 44,212,824-44,784,639 , GRCh38.p12 chr17: 46,135,458-46,707,273 , GRCh38.p12 chr17\|NT_187663.1: 837,565-1,226,699	DND1P2, RN7SL656P, 14 more genes
nsv4371571	copy number variation	1	nstd173	human		GRCh37 chr14: 106,693,454-106,751,190 , GRCh38.p12 chr14: 106,236,841-106,294,595	IGHV3-22, IGHVIII-22-2, 8 more genes
nsv4377438	copy number variation	4	nstd173	human		GRCh37 chrX: 116,861,624-116,890,818 , GRCh38.p12 chrX: 117,727,661-117,756,855	0
nsv4368473	copy number variation	289	nstd173	human		GRCh37 chr22: 42,918,351-42,943,641 , GRCh38.p12 chr22: 42,522,345-42,547,635	0

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