MS18406 AND nstd71 - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv890816	copy number variation	21	nstd71	human		NCBI36 chr8: 39,421,344-39,497,557 , GRCh37.p13 chr8: 39,302,187-39,378,400 , GRCh38.p12 chr8: 39,444,668-39,520,881	ADAM3A
nsv888900	copy number variation	27	nstd71	human		NCBI36 chr7: 102,032,517-102,062,128 , GRCh37.p13 chr7: 102,245,449-102,274,889 , GRCh38.p12 chr7: 102,605,002-102,634,442	RASA4
nsv885941	copy number variation	2	nstd71	human		NCBI36 chr6: 57,688,739-57,828,508 , GRCh37.p13 chr6: 57,580,780-57,720,549 , GRCh38.p12 chr6: 60,613,033-60,752,802	GAPDHP41
nsv893231	copy number variation	140	nstd71	human		NCBI36 chr9: 43,594,114-43,641,682 , GRCh37.p13 chr9: 43,654,118-43,701,686 , GRCh38.p12 chr9: 42,112,703-42,160,271	CNTNAP3B
nsv879242	copy number variation	10	nstd71	human		NCBI36 chr4: 69,047,457-69,126,340 , GRCh37.p13 chr4: 69,364,862-69,443,745 , GRCh38.p12 chr4: 68,499,144-68,578,027	UGT2B17, UGT2B29P
nsv895761	copy number variation	319	nstd71	human		NCBI36 chr10: 81,462,715-81,497,813 , GRCh37.p13 chr10: 81,472,521-81,507,631 , GRCh38.p12 chr10: 79,712,765-79,747,875	NUTM2B, NUTM2B-AS1
nsv895277	copy number variation	2	nstd71	human		NCBI36 chr10: 47,029,909-47,129,146 , GRCh37.p13 chr10: 47,559,903-47,659,140 , GRCh37.p13 chr10\|NW_003871068.1: 459,782-559,019 , GRCh38.p12 chr10: 46,188,667-46,287,904	AHCYP1, LOC105378577, 2 more genes
nsv899007	copy number variation	1	nstd71	human		NCBI36 chr12: 36,858,233-37,088,013 , GRCh37.p13 chr12: 38,571,966-38,801,746 , GRCh38.p12 chr12: 38,178,164-38,407,944	NF1P12, ALG10B, 2 more genes
nsv878213	copy number variation	1	nstd71	human		NCBI36 chr3: 199,119,920-199,251,908 , GRCh37.p13 chr3: 197,635,523-197,767,511 , GRCh38.p12 chr3: 197,908,652-198,040,640	RNU6-621P, RPL35A, 3 more genes
nsv879359	copy number variation	1	nstd71	human		NCBI36 chr4: 69,129,446-69,195,500 , GRCh37.p13 chr4: 69,446,851-69,512,905 , GRCh38.p12 chr4: 68,581,133-68,647,187	UGT2B15, LOC100422402, 2 more genes
nsv883574	copy number variation	5	nstd71	human		NCBI36 chr6: 29,957,666-29,980,430 , GRCh37.p13 chr6: 29,849,687-29,872,451 , GRCh38.p12 chr6: 29,881,910-29,904,674	DDX39BP1, HCG4P7, 2 more genes
nsv883916	copy number variation	5	nstd71	human		NCBI36 chr6: 29,988,619-30,003,090 , GRCh37.p13 chr6\|NT_167246.1: 1,174,816-1,189,318 , GRCh37.p13 chr6: 29,880,640-29,895,111 , GRCh38.p12 chr6: 29,912,863-29,927,334 , GRCh38.p12 chr6\|NT_167246.2: 1,169,196-1,183,698	HLA-A, HCG4B, 1 more genes
nsv893278	copy number variation	148	nstd71	human		NCBI36 chr9: 43,616,717-44,683,090 , GRCh37.p13 chr9: 43,676,721-44,743,094 , GRCh38.p12 chr9: 41,912,139-42,974,549	RBM17P3, RNU6-599P, 30 more genes
nsv907802	copy number variation	13	nstd71	human		NCBI36 chr17: 18,858,049-19,040,640 , GRCh37.p13 chr17: 18,917,324-19,100,047 , GRCh38.p12 chr17: 19,014,011-19,196,734	KYNUP1, SNORD3A, 11 more genes
nsv884258	copy number variation	146	nstd71	human		NCBI36 chr6: 31,388,306-31,398,785 , GRCh37.p13 chr6\|NT_167249.1: 2,614,037-2,624,528 , GRCh37.p13 chr6: 31,280,327-31,290,806 , GRCh38.p12 chr6: 31,312,550-31,323,029 , GRCh38.p12 chr6\|NT_167249.2: 2,614,739-2,625,230	0
nsv903247	copy number variation	118	nstd71	human		NCBI36 chr15: 19,635,853-20,203,694 , GRCh37.p13 chr15: 21,371,194-22,652,330 , GRCh38.p12 chr15: 21,165,865-22,308,242	OR11J6P, LOC642131, 56 more genes
nsv902781	copy number variation	11	nstd71	human		NCBI36 chr15: 19,031,743-19,488,393 , GRCh37.p13 chr15: 20,771,729-22,141,158 , GRCh38.p12 chr15: 20,566,406-21,498,353	LOC112268154, VN1R61P, 39 more genes
nsv885953	copy number variation	1	nstd71	human		NCBI36 chr6: 57,905,511-58,252,516 , GRCh37.p13 chr6: 57,797,552-58,144,557 , GRCh38.p12 chr: NaN-NaN	0
nsv898991	copy number variation	4	nstd71	human		NCBI36 chr12: 36,392,400-36,696,954 , GRCh37.p13 chr12: 38,106,133-38,410,687 , GRCh38.p12 chr12: 37,712,331-38,016,885	0

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