IS36678 AND nstd71 - dbVar - NCBI

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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
nsv891487	copy number variation	3	nstd71	human		NCBI36 chr8: 137,747,933-137,946,524 , GRCh37.p13 chr8: 137,678,751-137,877,342 , GRCh38.p12 chr8: 136,666,508-136,865,099	LINC02055
nsv872711	copy number variation	17	nstd71	human		NCBI36 chr1: 187,795,566-187,886,901 , GRCh37.p13 chr1: 189,528,943-189,620,278 , GRCh38.p12 chr1: 189,559,813-189,651,148	LOC105371657
nsv886250	copy number variation	523	nstd71	human		NCBI36 chr6: 79,022,244-79,098,352 , GRCh37.p13 chr6: 78,965,525-79,041,633 , GRCh38.p12 chr6: 78,255,808-78,331,916	LOC105377865
nsv890368	copy number variation	1	nstd71	human		NCBI36 chr8: 11,708,450-11,755,937 , GRCh37.p13 chr8: 11,671,041-11,718,528 , GRCh38.p12 chr8\|NW_018654717.1: 1,487,044-1,534,563 , GRCh38.p12 chr8: 11,813,532-11,861,019	FDFT1, CTSB
nsv880475	copy number variation	143	nstd71	human		NCBI36 chr5: 32,137,157-32,205,304 , GRCh37.p13 chr5: 32,101,400-32,169,547 , GRCh38.p12 chr5: 32,101,294-32,169,441	PDZD2, GOLPH3
nsv881025	copy number variation	1	nstd71	human		NCBI36 chr5: 36,610,778-36,648,810 , GRCh37.p13 chr5: 36,575,021-36,613,053 , GRCh38.p12 chr5: 36,574,919-36,612,951	SLC1A3, RPL39P22
nsv911912	copy number variation	43	nstd71	human		NCBI36 chr19: 48,060,801-48,160,500 , GRCh37.p13 chr19: 43,368,961-43,468,660 , GRCh38.p12 chr19: 42,864,809-42,964,508	CEACAMP7, PSG1, 2 more genes
nsv898668	copy number variation	46	nstd71	human		NCBI36 chr12: 7,884,583-8,005,696 , GRCh37.p13 chr12: 7,993,316-8,114,429 , GRCh38.p12 chr12: 7,840,720-7,961,833	RPS20P29, LOC100130582, 3 more genes
nsv883817	copy number variation	27	nstd71	human		NCBI36 chr6: 29,978,470-29,999,029 , GRCh37.p13 chr6\|NT_167246.1: 1,164,662-1,185,304 , GRCh37.p13 chr6: 29,870,491-29,891,050 , GRCh38.p12 chr6: 29,902,714-29,923,273 , GRCh38.p12 chr6\|NT_167246.2: 1,159,042-1,179,684	HLA-K, HCG4B, 4 more genes

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