M2290 AND nstd157 - dbVar - NCBI

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3317795	copy number variation	1	nstd157	human		GRCh37 chr10: 68,454,810-68,515,630 , GRCh38.p12 chr10: 66,695,052-66,755,872	CTNNA3
nsv3318787	copy number variation	1	nstd157	human		GRCh37 chr9: 20,072,967-20,101,896 , GRCh38.p12 chr9: 20,072,969-20,101,898	SLC24A2
nsv3318254	copy number variation	26	nstd157	human		GRCh37 chr13: 69,247,022-69,267,981 , GRCh38.p12 chr13: 68,672,890-68,693,849	RN7SL761P
nsv3318438	copy number variation	1	nstd157	human		GRCh37 chr11: 29,379,941-29,388,591 , GRCh38.p12 chr11: 29,358,394-29,367,044	LINC02755
nsv3318163	copy number variation	1	nstd157	human		GRCh37 chr3: 118,730,933-118,822,359 , GRCh38.p12 chr3: 119,012,086-119,103,512	IGSF11
nsv3317651	copy number variation	14	nstd157	human		GRCh37 chr3: 195,458,723-195,467,820 , GRCh38.p12 chr3: 195,731,852-195,740,949 , GRCh38.p12 chr3\|NT_187678.1: 55,095-64,192 , GRCh38.p12 chr3\|NT_187688.1: 53,782-62,847 , GRCh38.p12 chr3\|NT_187689.1: 102,349-111,446 , GRCh38.p12 chr3\|NT_187690.1: 53,786-62,854 , GRCh38.p12 chr3\|NT_187691.1: 53,898-63,024 , GRCh38.p12 chr3\|NT_187532.1: 102,349-111,446 , GRCh38.p12 chr3\|NT_187649.1: 53,782-62,847	MUC20
nsv3317919	copy number variation	3	nstd157	human		GRCh38.p12 chr1: 13,104,255-13,122,425 , GRCh37 chr1: 13,171,723-13,189,898	HNRNPCL2, PRAMEF35P
nsv3318734	copy number variation	11	nstd157	human		GRCh38.p12 chr19: 53,015,494-53,045,697 , GRCh37 chr19: 53,518,747-53,548,950	ERVV-1, ERVV-2
nsv3318672	copy number variation	1	nstd157	human		GRCh37 chr20: 61,710,473-61,727,599 , GRCh38.p12 chr20: 63,079,121-63,096,247	LINC01749, HAR1B
nsv3318745	copy number variation	44	nstd157	human		GRCh37 chr17: 34,438,753-34,483,342 , GRCh38.p12 chr17: 36,111,360-36,155,969 , GRCh38.p12 chr17\|NT_187661.1: 65,457-110,066 , GRCh38.p12 chr17\|NT_187614.1: 346,281-390,870	LOC100419980, LOC101927369, 2 more genes
nsv3317318	copy number variation	3	nstd157	human		GRCh38.p12 chr22: 42,512,492-42,554,027 , GRCh37 chr22: 42,908,498-42,950,033	RRP7A, SERHL, 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
nsv3317289	copy number variation	24	nstd157	human		GRCh37 chr9: 24,502,737-24,518,795 , GRCh38.p12 chr9: 24,502,739-24,518,797	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
nsv3317118	copy number variation	1	nstd157	human		GRCh37 chr7: 46,699,079-46,723,510 , GRCh38.p12 chr7: 46,659,481-46,683,912	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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