210240 AND nstd173 - dbVar - NCBI

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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
nsv4387797	copy number variation	78	nstd173	human		GRCh37 chr1: 72,773,260-72,812,440 , GRCh38.p12 chr1: 72,307,577-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 19,844-67,982	LOC105378797
nsv4370970	copy number variation	2	nstd173	human		GRCh37 chr6: 320,859-381,137 , GRCh38.p12 chr6: 320,859-381,137	DUSP22
nsv4370116	copy number variation	174	nstd173	human		GRCh37 chr2: 98,138,417-98,161,960 , GRCh38.p12 chr2: 97,521,954-97,545,497	ANKRD36B
nsv4376437	copy number variation	46	nstd173	human		GRCh37 chr12: 11,503,156-11,553,849 , GRCh38.p12 chr12: 11,350,222-11,400,915 , GRCh38.p12 chr12\|NT_187658.1: 545,185-572,349	PRB1, PRB2
nsv4367142	copy number variation	135	nstd173	human		GRCh37 chr12: 2,235,941-2,259,954 , GRCh38.p12 chr12: 2,126,775-2,150,788 , GRCh38.p12 chr12\|NW_018654718.1: 468,919-492,932	LOC107984131, CACNA1C
nsv4376724	copy number variation	112	nstd173	human		GRCh37 chr8: 39,246,772-39,397,015 , GRCh38.p12 chr8: 39,389,253-39,539,496	ADAM5, ADAM3A
nsv4369602	copy number variation	1	nstd173	human		GRCh37 chr8: 130,792,203-130,852,228 , GRCh38.p12 chr8: 129,779,957-129,839,982 , GRCh38.p12 chr8\|NW_019805494.1: 64,330-103,072	CYRIB, GSDMC
nsv4384996	copy number variation	2	nstd173	human		GRCh37 chrY: 25,415,736-25,609,620 , GRCh38.p12 chrY: 23,269,589-23,463,473	PPP1R12BP2, REREP1Y, 2 more genes
nsv4381562	copy number variation	367	nstd173	human		GRCh37 chr11: 55,374,019-55,453,008 , GRCh38.p12 chr11: 55,606,543-55,685,532	OR4P1P, OR4C6, 3 more genes
nsv4376755	copy number variation	329	nstd173	human		GRCh37 chr14: 74,001,122-74,024,031 , GRCh38.p12 chr14: 73,534,418-73,557,327	ACOT1, NT5CP2, 1 more genes
nsv4378235	copy number variation	17	nstd173	human		GRCh37 chr5: 180,378,776-180,430,789 , GRCh38.p12 chr5: 180,951,776-181,003,789	TMEM69P2, LOC100128762, 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
nsv4380701	copy number variation	12	nstd173	human		GRCh37 chrY: 25,844,786-26,158,899 , GRCh38.p12 chrY: 23,698,639-24,012,752	RNU1-97P, USP9YP13, 18 more genes
nsv4378128	copy number variation	463	nstd173	human		GRCh37 chr11: 51,337,076-51,376,963 , GRCh38.p12 chr11: 54,742,317-54,782,204	0
nsv4368229	copy number variation	1	nstd173	human		GRCh37 chr22: 18,649,190-19,024,659 , GRCh38.p12 chr22: 18,166,423-19,037,146	POM121L15P, GGTLC3, 31 more genes
nsv4382819	copy number variation	1	nstd173	human		GRCh37 chr14: 22,441,153-22,970,223 , GRCh38.p12 chr14: 21,972,924-22,501,239	TRAV35, TRAJ39, 70 more genes
nsv4378591	copy number variation	3	nstd173	human		GRCh37 chr7: 142,226,368-142,493,638 , GRCh38.p12 chr7: 142,618,685-142,785,829 , GRCh38.p12 chr7\|NT_187562.1: 622,348-808,802	PRSS3P1, WBP1LP1, 24 more genes
nsv4367958	copy number variation	71	nstd173	human		GRCh37 chr7: 38,293,950-38,378,483 , GRCh38.p12 chr7: 38,254,349-38,338,882	TRG, TRGV11, 15 more genes
nsv4377396	copy number variation	94	nstd173	human		GRCh37 chr14: 106,536,991-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

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