196902 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
nsv4372152	copy number variation	236	nstd173	human		GRCh37 chr6: 78,969,092-79,035,184 , GRCh38.p12 chr6: 78,259,375-78,325,467	LOC105377865
nsv4373337	copy number variation	44	nstd173	human		GRCh37 chr2: 98,063,359-98,162,176 , GRCh38.p12 chr2: 97,490,656-97,545,713	ANKRD36B
nsv4368058	copy number variation	90	nstd173	human		GRCh37 chr5: 97,043,561-97,093,733 , GRCh38.p12 chr5: 97,707,857-97,758,029	LOC391813
nsv4376284	copy number variation	379	nstd173	human		GRCh37 chr14: 41,608,616-41,657,457 , GRCh38.p12 chr14: 41,139,413-41,188,254	LINC02315
nsv4384091	copy number variation	77	nstd173	human		GRCh37 chr11: 49,710,704-49,746,720 , GRCh38.p12 chr11: 49,689,152-49,725,168 , GRCh38.p12 chr11\|NW_019805495.1: 153,334-179,145	GRM5P1
nsv4373514	copy number variation	2	nstd173	human		GRCh37 chr14: 44,498,365-44,532,098 , GRCh38.p12 chr14: 44,029,162-44,062,895	LINC02307
nsv4369227	copy number variation	203	nstd173	human		GRCh37 chr1: 72,771,366-72,811,904 , GRCh38.p12 chr1: 72,305,683-72,346,221 , GRCh38.p12 chr1\|NW_018654707.1: 17,950-67,446	LOC105378797
nsv4384457	copy number variation	635	nstd173	human		GRCh37 chr11: 55,374,031-55,453,008 , GRCh38.p12 chr11: 55,606,555-55,685,532	OR4P1P, OR4C6, 3 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
nsv4376452	copy number variation	337	nstd173	human		GRCh37 chr17: 34,437,494-34,477,480 , GRCh38.p12 chr17: 36,110,101-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,198-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,022-385,008	LOC101927369, LOC107985055, 3 more genes
nsv4368670	copy number variation	15	nstd173	human		GRCh37 chr5: 140,218,726-140,252,247 , GRCh38.p12 chr5: 140,839,141-140,872,662	PCDHA6, PCDHA10, 12 more genes
nsv4382392	copy number variation	421	nstd173	human		GRCh37 chr3: 65,185,849-65,210,375 , GRCh38.p12 chr3: 65,200,174-65,224,700	0
nsv4368660	copy number variation	868	nstd173	human		GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0
nsv4369404	copy number variation	213	nstd173	human		GRCh37 chr14: 107,150,444-107,179,594 , GRCh38.p12 chr14: 106,694,427-106,771,352	IGHV2-70, IGH, 7 more genes
nsv4380336	copy number variation	14	nstd173	human		GRCh37 chr14: 106,525,299-106,849,677 , GRCh38.p12 chr14: 106,069,054-106,393,766 , GRCh38.p12 chr14\|NT_187600.1: 502,910-1,214,078	IGHV3-23, IGHV3-54, 113 more genes

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