SP53399 AND nstd71 - dbVar - NCBI

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv895630	copy number variation	1	nstd71	human		NCBI36 chr10: 67,954,023-68,065,930 , GRCh37.p13 chr10: 68,284,017-68,395,924 , GRCh38.p12 chr10: 66,524,259-66,636,166	CTNNA3
nsv885085	copy number variation	2	nstd71	human		NCBI36 chr6: 32,606,992-32,625,376 , GRCh37.p13 chr6\|NT_167247.1: 3,864,568-3,875,071 , GRCh37.p13 chr6\|NT_167246.1: 3,827,971-3,838,799 , GRCh37.p13 chr6: 32,499,014-32,517,398 , GRCh37.p13 chr6\|NT_167249.1: 3,832,679-3,843,181 , GRCh38.p12 chr6\|NT_167249.2: 3,833,381-3,843,883 , GRCh38.p12 chr6: 32,531,237-32,549,621 , GRCh38.p12 chr6\|NT_167247.2: 3,858,983-3,869,486	RNU1-61P
nsv890754	copy number variation	920	nstd71	human		NCBI36 chr8: 39,350,791-39,509,376 , GRCh37.p13 chr8: 39,231,634-39,390,219 , GRCh38.p12 chr8: 39,374,115-39,532,700	ADAM5, ADAM3A
nsv912880	copy number variation	1	nstd71	human		NCBI36 chr20: 40,671,918-40,730,408 , GRCh37.p13 chr20: 41,238,504-41,296,994 , GRCh38.p12 chr20: 42,609,864-42,668,354	LOC105372624, PTPRT
nsv897658	copy number variation	1	nstd71	human		NCBI36 chr11: 63,567,520-63,654,335 , GRCh37.p13 chr11: 63,810,944-63,897,759 , GRCh38.p12 chr11: 64,043,472-64,130,287	FLRT1, MACROD1
nsv891173	copy number variation	8	nstd71	human		NCBI36 chr8: 89,578,339-90,065,906 , GRCh37.p13 chr8: 89,509,223-89,996,790 , GRCh38.p12 chr8: 88,496,994-88,984,561	LOC105375629, LOC105375631, 1 more genes
nsv879310	copy number variation	1929	nstd71	human		NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558	LOC100422402, LOC100132651, 2 more genes
nsv883741	copy number variation	25	nstd71	human		NCBI36 chr6: 29,972,294-29,988,619 , GRCh37.p13 chr6\|NT_167246.1: 1,158,492-1,174,816 , GRCh37.p13 chr6: 29,864,315-29,880,640 , GRCh38.p12 chr6\|NT_167246.2: 1,152,872-1,169,196 , GRCh38.p12 chr6: 29,896,538-29,912,863	HLA-T, MCCD1P1, 3 more genes
nsv904023	copy number variation	257	nstd71	human		NCBI36 chr15: 32,487,589-32,625,184 , GRCh37.p13 chr15: 34,700,297-34,837,892 , GRCh38.p12 chr15: 34,408,096-34,545,691	LOC100422491, GOLGA8B, 5 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
nsv884638	copy number variation	2	nstd71	human		NCBI36 chr6: 32,072,225-32,089,979 , GRCh37.p13 chr6\|NT_167249.1: 3,296,956-3,314,711 , GRCh37.p13 chr6: 31,964,246-31,982,001 , GRCh37.p13 chr6\|NT_167245.1: 3,249,828-3,267,584 , GRCh38.p12 chr6\|NT_167249.2: 3,297,658-3,315,413 , GRCh38.p12 chr6: 31,996,469-32,014,224 , GRCh38.p12 chr6\|NT_167245.2: 3,244,243-3,261,999	C4A, C4B, 4 more genes
nsv901296	copy number variation	150	nstd71	human		NCBI36 chr14: 19,261,709-19,494,891 , GRCh37.p13 chr14: 20,191,869-20,425,051 , GRCh38.p12 chr14: 19,723,710-19,956,892	OR4K16P, OR4K2, 12 more genes
nsv902543	copy number variation	11	nstd71	human		NCBI36 chr14: 105,118,950-105,259,090 , GRCh37.p13 chr14\|NW_004166863.1: 244,735-384,875 , GRCh37.p13 chr14: 106,047,905-106,188,045 , GRCh38.p12 chr14\|NT_187600.1: 72,812-189,477 , GRCh38.p12 chr14: 105,605,043-105,721,708	IGHGP, , 10 more genes

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SP53399 AND nstd71 (14)
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Same, Connectivity for PubChem Compound (Select 129320472) (1)
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Assembly links for BioSample (Select 6454038) (1)
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