150331 AND nstd173 - 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
nsv4381259	copy number variation	27	nstd173	human		GRCh37 chr8: 3,769,850-3,790,036 , GRCh38.p12 chr8: 3,912,328-3,932,514	CSMD1
nsv4382665	copy number variation	2	nstd173	human		GRCh37 chr12: 86,971,755-87,022,758 , GRCh38.p12 chr12: 86,577,978-86,628,981	MGAT4C
nsv4385455	copy number variation	190	nstd173	human		GRCh37 chr20: 1,557,177-1,597,997 , GRCh38.p12 chr20: 1,576,531-1,617,351	SIRPB1
nsv4366274	copy number variation	133	nstd173	human		GRCh37 chr7: 75,354,113-75,375,909 , GRCh38.p12 chr7: 75,724,795-75,746,591	HIP1
nsv4376456	copy number variation	1782	nstd173	human		GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445	ADAM5, ADAM3A
nsv4372080	copy number variation	569	nstd173	human		GRCh37 chr1: 72,762,663-72,812,440 , GRCh38.p12 chr1: 72,296,980-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,982	RPL31P12, LOC105378797
nsv4376403	copy number variation	119	nstd173	human		GRCh37 chr19: 53,517,242-53,553,087 , GRCh38.p12 chr19: 53,013,989-53,049,834	ERVV-1, ERVV-2
nsv4372113	copy number variation	10	nstd173	human		GRCh37 chr14: 48,787,824-48,913,473 , GRCh38.p12 chr14: 48,318,621-48,444,270	LOC100422641, RNU6-297P, 1 more genes
nsv4374028	copy number variation	1	nstd173	human		GRCh37 chr6: 10,495,236-10,575,131 , GRCh38.p12 chr6: 10,495,003-10,574,898 , GRCh38.p12 chr6\|NW_018654713.1: 5,887-85,782	GCNT2, RPL21P63, 2 more genes
nsv4379351	copy number variation	123	nstd173	human		GRCh37 chr19: 51,321,391-51,345,568 , GRCh38.p12 chr19: 50,818,135-50,842,312	LOC105372441, KLK1, 2 more genes
nsv4368241	copy number variation	217	nstd173	human		GRCh37 chr17: 34,437,482-34,477,480 , GRCh38.p12 chr17: 36,110,089-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,186-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,010-385,008	LOC100419980, LOC101927369, 3 more genes
nsv4367001	copy number variation	197	nstd173	human		GRCh37 chr14: 74,001,111-74,024,031 , GRCh38.p12 chr14: 73,534,407-73,557,327	NT5CP2, ACOT1, 1 more genes
nsv4377904	copy number variation	28	nstd173	human		GRCh37 chr19: 20,596,118-20,720,868 , GRCh38.p12 chr19: 20,413,312-20,538,062	ZNF826P, ZNF737, 4 more genes
nsv4369570	copy number variation	1	nstd173	human		GRCh37 chr14: 22,461,404-22,975,700 , GRCh38.p12 chr14: 21,993,164-22,506,715	TRDD1, TRAJ38, 73 more genes
nsv4385529	copy number variation	179	nstd173	human		GRCh37 chr14: 106,525,299-106,692,891 , GRCh38.p12 chr14: 106,069,054-106,236,281 , GRCh38.p12 chr14\|NT_187600.1: 536,823-704,050	IGHVIII-13-1, IGHV1-18, 19 more genes
nsv4366173	copy number variation	39	nstd173	human		GRCh37 chr7: 142,266,307-142,475,287 , GRCh38.p12 chr7: 142,618,685-142,732,123 , GRCh38.p12 chr7\|NT_187562.1: 656,734-770,033	TRBV27, TRBV24-1, 16 more genes
nsv4376615	copy number variation	31	nstd173	human		GRCh37 chr7: 38,294,088-38,378,483 , GRCh38.p12 chr7: 38,254,487-38,338,882	TRGJP, TRGV7, 15 more genes
nsv4384649	copy number variation	1	nstd173	human		GRCh37 chr12: 87,381,076-87,428,601 , GRCh38.p12 chr12: 86,987,299-87,034,824 , GRCh38.p12 chr12\|NW_015148967.1: 218,921-266,446	0
nsv4387382	copy number variation	84	nstd173	human		GRCh37 chr5: 57,326,026-57,349,970 , GRCh38.p12 chr5: 58,030,199-58,054,143	0

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